| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1056/NEJM198112313052704 |
| P698 | PubMed publication ID | 6796886 |
| P2093 | author name string | Riccardi VM | |
| P433 | issue | 27 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 11 | |
| P304 | page(s) | 1617-1627 | |
| P577 | publication date | 1981-12-01 | |
| P1433 | published in | The New England Journal of Medicine | Q582728 |
| P1476 | title | Von Recklinghausen neurofibromatosis | |
| P478 | volume | 305 |
| Q70286156 | A case of a thoracic vertebral body dislocation without neurological signs in a child with neurofibromatosis |
| Q44307732 | A cell culture study on melanocytes from patients with neurofibromatosis-1. |
| Q49145045 | A clinical study of vestibular schwannomas in type 2 neurofibromatosis |
| Q33921397 | A contribution to the differential diagnosis of the "group of schizophrenias": structural abnormality of chromosome 4 |
| Q30495392 | A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity |
| Q24514960 | A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity |
| Q73963842 | A hemorrhagic complication of neurofibromatosis |
| Q74143794 | A rapidly growing benign intrathoracic neurofibroma after lung lobectomy |
| Q38245661 | A review of astrocytoma in childhood |
| Q39274330 | Abdominal mass in a 19-year-old with neurofibromatosis |
| Q38757104 | Aberrant Myeloid Differentiation Contributes to the Development of Osteoporosis in Neurofibromatosis Type 1. |
| Q41888950 | Achalasia like disorder of the oesophagus in von Recklinghausen's neurofibromatosis |
| Q67281578 | Acute renal insufficiency due to renal infarctions in a patient with neurofibromatosis |
| Q30544224 | Adrenal medullary tumors and iris proliferation in a transgenic mouse model of neurofibromatosis |
| Q78679609 | Advances in the surgical management of sarcomas in children |
| Q69448392 | Agminated neurilemomas |
| Q42048048 | Altered calcium-mediated cell signaling in keratinocytes cultured from patients with neurofibromatosis type 1. |
| Q71130409 | Ampullary somatostatinoma associated with von Recklinghausen's neurofibromatosis presenting as obstructive jaundice |
| Q71311714 | Ampullary somatostatinoma in a patient with von Recklinghausen's disease |
| Q42846844 | Ampullary somatostatinomas and jejunal gastrointestinal stromal tumor in a patient with Von Recklinghausen's disease |
| Q48495719 | An intracranial leiomyosarcoma in a child with neurofibromatosis type 1. |
| Q47957444 | Analysis of vascularity of human neurofibromas |
| Q54779321 | At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case series. |
| Q67695559 | Axons induce differentiation of neurofibroma Schwann-like cells |
| Q70500716 | Basement membrane components in cutaneous neurofibroma of von Recklinghausen's disease |
| Q33971598 | Behavioral phenotype of neurofibromatosis, type 1. |
| Q67912327 | Benign spinal nerve sheath tumors: their occurrence sporadically and in neurofibromatosis types 1 and 2 |
| Q70480501 | Bilateral dermatomal neurofibromatosis |
| Q34394162 | Bilateral segmental neurofibromatosis: a case report and review |
| Q76390691 | Blood pressure and cardiovascular involvement in children with neurofibromatosis type1 |
| Q46292236 | Bone mineral metabolism in patients with neurofibromatosis type 1 (von Recklingausen disease). |
| Q35602625 | Brain revascularisation in hypertension |
| Q71402678 | Bronchoalveolar lavage cytology in pulmonary fibrosis associated with neurofibromatosis |
| Q42461922 | Buschke-Ollendorff Syndrome Associated with Elevated Elastin Production by Affected Skin Fibroblasts in Culture |
| Q36431277 | CO2 laser treatment of cutaneous neurofibromas |
| Q57394335 | COGNITIVE FUNCTION AND ACADEMIC PERFORMANCE IN CHILDREN WITH NEUROFIBROMATOSIS TYPE 1 |
| Q39810108 | Can linkage and marker association resolve the genetic aetiology of psychiatric disorders? Review and argument |
| Q28278854 | Cancer phenomics: RET and PTEN as illustrative models |
| Q77156377 | Cardiac abnormalities detected by Doppler imaging in patients with neurofibromatosis type 1 |
| Q72443040 | Case report 828: Plexiform neurofibroma of the tibial nerve invading the medial and lateral gastrocnemius muscles and plantaris muscle |
| Q70434166 | Cell culture studies on neurofibromatosis (von Recklinghausen). II. Occurrence of glial cells in primary cultures of peripheral neurofibromas |
| Q69967460 | Cell-culture studies on neurofibromatosis (von Recklinghausen's disease). III. Experiments on X-ray sensitivity |
| Q55480074 | Cerebro-vasculopathy and malignancy: catastrophic complications of radiotherapy for optic nerve glioma in a von Recklinghausen neurofibromatosis patient. |
| Q72307592 | Cervical neurofibroma in a patient with von Recklinghausen's disease |
| Q41382108 | Cervical vertebral arteriovenous fistula balloon embolization in a patient with neurofibromatosis type 1. |
| Q74454260 | Characterization of Pheochromocytomas in a Mouse Strain with a Targeted Disruptive Mutation of the Neurofibromatosis Gene Nf1 |
| Q35834025 | Characterization of naturally occurring cutaneous neurofibromatosis in Holstein cattle. A disorder resembling neurofibromatosis type 1 in humans. |
| Q39624893 | Cholecystitis, cholelithiasis, and ganglioneuromatosis of the gall bladder: an unusual presentation of MEN type 2b. |
| Q35831788 | Chromosomal and genetic forms of growth failure |
| Q30531015 | Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis |
| Q68353287 | Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study |
| Q30503427 | Clinical and genetic patterns of neurofibromatosis 1 and 2. |
| Q36234581 | Clinical and pathologic features of familial interstitial pneumonia |
| Q37087817 | Clinical features of paraganglioma syndromes |
| Q33593848 | Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? |
| Q41820871 | Colonic obstruction in a child with von Recklinghausen's neurofibromatosis |
| Q55488789 | Combined clinical and computed tomographic diagnosis of orbital glioma and meningioma. |
| Q31142656 | Comparative study of CO2- and Er:YAG laser ablation of multiple cutaneous neurofibromas in von Recklinghausen's disease |
| Q24794175 | Complex splicing pattern generates great diversity in human NF1 transcripts |
| Q34599389 | Concomitant compostite adrenal phoechromocytoma, multipte gastric stromal tumours and pseudohermaphrodism in a patient with von Recklinghausen's disease |
| Q80350300 | Congenital (infantile) pseudarthrosis of the fibula associated with osteofibrous dysplasia |
| Q46575531 | Constitutional p53 mutations associated with brain tumors in young adults |
| Q52622505 | Contributions of inflammation and tumor microenvironment to neurofibroma tumorigenesis. |
| Q35889608 | Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies. |
| Q35198839 | DNA "fingerprints" and segregation analysis of multiple markers in human pedigrees |
| Q48208978 | Development of anaplastic changes in low-grade astrocytomas of childhood |
| Q51979366 | Diagnosing genetic anomalies by inspection. |
| Q50667667 | Diagnosis and Management of Hereditary Phaeochromocytoma and Paraganglioma. |
| Q38544014 | Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation |
| Q36198617 | Diagnosis and treatment options for nerve sheath tumors |
| Q48193085 | Diet and serum markers in relation to primary brain tumor risk in China |
| Q48414920 | Diffuse leptomeningeal seeding from a malignant spinal cord astrocytoma in a child with neurofibromatosis |
| Q56394872 | Diffuse lung disease associated with neurofibromatosis type-1 can also affect children |
| Q37950848 | Diffuse lung disease in neurofibromatosis |
| Q42327475 | Diffuse plexiform neurofibroma |
| Q49129728 | Disfluency: it is not always stuttering |
| Q34658446 | Double inactivation of NF1 in tibial pseudarthrosis |
| Q70325577 | Duodenal carcinoid in neurofibromatosis: a calcitonin- and amyloid-containing tumor |
| Q67726661 | Dysplastic nevi and the dysplastic nevus syndrome |
| Q35191542 | Dystrophic spinal deformities in a neurofibromatosis type 1 murine model |
| Q54577179 | EGF genetic polymorphism is associated with clinical features but not malignant phenotype in neurofibromatosis type 1 patients. |
| Q73852990 | Embolization of a ruptured intercostal artery aneurysm in type I neurofibromatosis |
| Q51605271 | Epidural analgesia for labour in a parturient with neurofibromatosis. |
| Q30666653 | Epilepsy in individuals with neurofibromatosis type 1. |
| Q34208209 | Epilepsy in neurofibromatosis 1. |
| Q72186689 | Extremity malignant peripheral nerve sheath tumors (neurogenic sarcomas): a 10-year experience |
| Q68081374 | Facial nerve neuromas: MR imaging. Report of four cases |
| Q70479576 | Failure to visualise renal artery stenosis secondary to neurofibromatosis 1 by Doppler ultrasound |
| Q34678023 | Familial Interstitial Pneumonia (FIP). |
| Q39637009 | Familial meningioma. Case report with cytogenetic study |
| Q33999722 | Familial neurofibromatosis and hypertrophic cardiomyopathy |
| Q72020505 | Fatal haemorrhage associated with neurofibromatosis |
| Q30541697 | Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22. |
| Q33181311 | Frequency of choroidal abnormalities in neurofibromatosis type 1. |
| Q24802460 | Functional expression of NF1 tumor suppressor protein: association with keratin intermediate filaments during the early development of human epidermis |
| Q42727043 | Further evidence of the increased risk for malignant peripheral nerve sheath tumour from a Scottish cohort of patients with neurofibromatosis type 1 |
| Q73816054 | Gains in chromosomes 7, 8q, 15q and 17q are characteristic changes in malignant but not in benign peripheral nerve sheath tumors from patients with Recklinghausen's disease |
| Q72127961 | Gastrointestinal autonomic nerve tumours and their separation from other gastrointestinal stromal tumours: an ultrastructural and immunohistochemical study of seven cases |
| Q35855118 | Gene expression profiling of familial and sporadic interstitial pneumonia |
| Q30841192 | Generalized metabolic bone disease in Neurofibromatosis type I |
| Q37103542 | Genetic analysis of sporadic and familial interstitial pneumonia |
| Q35247419 | Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I. |
| Q59076230 | Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22 |
| Q34010166 | Genetic predisposition to respiratory diseases: infiltrative lung diseases |
| Q40686977 | Genetics of primary brain tumors: a review |
| Q48611503 | Giant phaeochromocytoma presenting with an acute stroke: reappraising phaeochromocytoma surveillance for the neurofibromatosis type 1 phakomatosis. |
| Q36097981 | Gingival overgrowth in children: epidemiology, pathogenesis, and complications. A literature review |
| Q74063203 | Growth hormone deficiency in children with neurofibromatosis type 1 without suprasellar lesions |
| Q53775363 | Hamartoma of neural origin. |
| Q46158204 | Hemothorax in type I neurofibromatosis |
| Q36796929 | High-resolution ultrasound of peripheral neurogenic tumors. |
| Q39226839 | Histopathology, cytology and cytochemistry of pheochromocytomas and paragangliomas including chemodectomas |
| Q58136289 | How Common is Hereditary Cancer? |
| Q68339814 | Hypercalcemic hyperparathyroidism and hypophosphatemic osteomalacia complicating neurofibromatosis |
| Q69572512 | Idiopathic subcutaneous and laryngeal fibrosis |
| Q48147709 | Infantile spasms in patients with neurofibromatosis type 1. |
| Q38207155 | Intestinal obstruction in von Recklinghausen's disease |
| Q38550187 | Intra-abdominal plexiform neurofibromatosis including periportal, mesentery, and gastrointestinal tract involvement in neurofibromatosis type 1: case report and review of the literature |
| Q30495904 | Intracranial calcified deposits in neurofibromatosis |
| Q37919903 | Intracranial calcified deposits in neurofibromatosis type 2. A CT study of 11 cases |
| Q40213919 | Intraparotid hemangioma in an adult. Case report and review of the literature |
| Q71740784 | Intrathoracic dural ectasia mimicking neurofibroma and scoliosis. A case report |
| Q36277012 | Intrathoracic vagus nerve neurofibroma and sudden death in a patient with neurofibromatosis |
| Q69939514 | Investigation of the cytotoxic effects of DNA damaging agents on neurofibromatosis cells |
| Q77525543 | Ionizing radiation and genetic risks IX. Estimates of the frequencies of mendelian diseases and spontaneous mutation rates in human populations: a 1998 perspective |
| Q34091275 | Iris melanoma in a patient with neurofibromatosis |
| Q70166409 | Isolated neurofibromas of the conjunctiva |
| Q44494403 | Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infection |
| Q41416321 | Juvenile xanthogranuloma |
| Q50310983 | Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism |
| Q73690237 | Laparoscopic surgery for pheochromocytoma |
| Q38703164 | Laryngeal Manifestations of Neurofibromatosis |
| Q61811465 | Left colic artery aneurysm rupture after stent placement for abdominal aortic aneurysm associated with neurofibromatosis type 1 |
| Q42479827 | Lesional Psoriatic Epidermis Displays Reduced Neurofibromin Immunoreactivity |
| Q80492770 | Life-threatening gastrointestinal haemorrhage in Von Recklinghausen's disease |
| Q33675797 | Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis |
| Q33672386 | Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy. |
| Q30495414 | Linkage studies in peripheral neurofibromatosis. |
| Q34304607 | Loss of distinct regions on the short arm of chromosome 17 associated with tumorigenesis of human astrocytomas |
| Q71639478 | Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type I |
| Q74502557 | Loss of neurofibromin in the leptomeningeal astroglial heterotopia of NF-1 |
| Q74801033 | Losses in chromosomes 17, 19, and 22q in neurofibromatosis type 1 and sporadic neurofibromas: a comparative genomic hybridization analysis |
| Q71343975 | Lymphangiolipoma of the thoracic spine in a pediatric patient with Proteus syndrome |
| Q42492024 | MRI and CT evaluation of brain in neurofibromatosis. Case report |
| Q38612535 | Malignant hemangiopericytoma arising in neurofibromatosis: a case report with histological, immunohistochemical and ultrastructural studies |
| Q37477136 | Malignant peripheral nerve sheath tumor in neurofibromatosis type I: unusual presentation of intraabdominal or intrathoracic mass |
| Q70507405 | Malignant peripheral nerve sheath tumors in childhood |
| Q33904761 | Malignant peripheral nerve sheath tumors of the head and neck: analysis of prognostic factors |
| Q92592488 | Malignant peripheral nerve-sheath tumors in an adolescent patient with mosaic localized NF1: A case report |
| Q30893777 | Malignant pheochromocytoma: clinical, biological, histologic and therapeutic data in a series of 20 patients with distant metastases |
| Q40775265 | Malignant schwannoma of the parapharyngeal space in von Recklinghausen's disease: a case report and review of the literature. |
| Q34022409 | Mast cells and the neurofibroma microenvironment |
| Q41519725 | Maternal Genetic Disease and Pregnancy |
| Q51985744 | Math learning disability and math LD subtypes: evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1. |
| Q37467387 | Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1. |
| Q39641245 | Megalencephaly: definition and classification |
| Q37391841 | Mice lacking neurofibromin develop gastric hyperplasia |
| Q41942039 | Missing clues for a radiologist |
| Q43232503 | Mitotic recombination as evidence of alternative pathogenesis of gastrointestinal stromal tumours in neurofibromatosis type 1. |
| Q40468269 | Molecular Genetics and Cytogenetics of Sarcomas |
| Q37003276 | Molecular Genetics of von Recklinghausen Neurofibromatosis |
| Q73741067 | Monsters, myths and syndromes depicted on stamps |
| Q48497287 | Multiple causes of cerebrovascular events in children with tumors of the parasellar region |
| Q55463834 | Multiple endocrine neoplasia associated with von Recklinghausen's disease. |
| Q45148240 | Multiple gastrointestinal stromal tumors in type I neurofibromatosis: a pathologic and molecular study |
| Q54055358 | Multiple papillary adenomas of type II pneumocytes found in a 13-year-old boy with von Recklinghausen's disease. |
| Q30492334 | Multiple schwannomas: report of two cases |
| Q33682913 | Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas |
| Q33630439 | Myotonic dystrophy and hyperparathyroidism: association with neurofibromatosis and multiple endocrine adenomatosis type 2A. |
| Q87252798 | Myxoid perineurioma in a transplanted kidney |
| Q42795746 | NF1 modulates the effects of Ras oncogenes: evidence of other NF1 function besides its GAP activity |
| Q72526907 | NF1: a prevalent cause of tumorigenesis in human cancers? |
| Q69352721 | Nerve growth factor receptor immunoreactivity in human benign peripheral nerve sheath tumor |
| Q69361166 | Nerve sheath myxoma of the breast. A light and electron microscopic, histochemical and immunohistochemical study |
| Q48353438 | Neurilemmomatosis, NF2, and juvenile xanthogranuloma |
| Q70156914 | Neurilemoma of the retroperitoneum |
| Q40914446 | Neurocristopathy: its growth and development in 20 years |
| Q68217832 | Neurocutaneous syndromes |
| Q71822302 | Neurofibroma in the articular disc of the temporomandibular joint: a case report |
| Q30467554 | Neurofibromatosis |
| Q70356605 | Neurofibromatosis |
| Q86553170 | Neurofibromatosis 1 presenting with multiple duodenal GISTS associated with a somatostatin-producing D cell neoplasm |
| Q34982022 | Neurofibromatosis 1: clinical manifestations and diagnostic criteria |
| Q50692074 | Neurofibromatosis 1: recommendations for management |
| Q64261492 | Neurofibromatosis Type 1: Review of Cutaneous and Subcutaneous Tumor Treatment on Quality of Life |
| Q39503112 | Neurofibromatosis and associated neuroectodermal tumors: a congenital neurocristopathy |
| Q69227648 | Neurofibromatosis classification clarified |
| Q45757353 | Neurofibromatosis clinical presentations: A report of two cases |
| Q70480504 | Neurofibromatosis heterogeneity |
| Q58147495 | Neurofibromatosis in Children |
| Q56093335 | Neurofibromatosis type 1 |
| Q41510986 | Neurofibromatosis type 1 and male breast cancer: emerging risk factor? |
| Q36850523 | Neurofibromatosis type 1 and type 2: review of the central nervous system and related structures |
| Q37002779 | Neurofibromatosis type 1 associated with pheochromocytoma and gastrointestinal stromal tumors: A case report and literature review |
| Q41579794 | Neurofibromatosis type 1 gene mutations in neuroblastoma |
| Q33596184 | Neurofibromatosis type 1 in Israel: survey of young adults |
| Q30502676 | Neurofibromatosis type 1 in children |
| Q24299697 | Neurofibromatosis type 1 protein and amyloid precursor protein interact in normal human melanocytes and colocalize with melanosomes |
| Q41254273 | Neurofibromatosis type 1--an update and review for the primary pediatrician |
| Q34330612 | Neurofibromatosis type 1: II. Answers from animal models |
| Q47638775 | Neurofibromatosis type 1: a case highlighting pulmonary and other rare clinical manifestations. |
| Q28279834 | Neurofibromatosis type 1: piecing the puzzle together |
| Q40775106 | Neurofibromatosis type 1: review of the first 200 patients in an Australian clinic |
| Q50544031 | Neurofibromatosis type I--a rare case resulting in conductive hearing loss. |
| Q54412565 | Neurofibromatosis versus giant pigmented nevus. |
| Q80604617 | Neurofibromatosis with gastrointestinal stromal tumors: insights into the association |
| Q40988063 | Neurofibromatosis with involvement of the prostate gland |
| Q42476299 | Neurofibromatosis, stroke and basilar impression. Case report |
| Q35885643 | Neurofibromatosis, von Recklinghausen's disease, multiple schwannomas, malignant schwannomas. Multiple schwannomas in the bicolor damselfish, Pomacentrus partitus (pisces, pomacentridae). |
| Q40266828 | Neurofibromatosis: clinical heterogeneity |
| Q34958103 | Neurofibromatosis: implications for the general surgeon |
| Q48417018 | Neurofibromin, a predominantly neuronal GTPase activating protein in the adult, is ubiquitously expressed during development |
| Q79605117 | Neurofibromin-deficient Schwann cells have increased lysophosphatidic acid dependent survival and migration-implications for increased neurofibroma formation during pregnancy |
| Q33788873 | Neurofibromin-deficient fibroblasts fail to form perineurium in vitro |
| Q45305265 | Neurologic Examination of Children with Learning Disorders |
| Q52214056 | Neuropsychological profile of children with neurofibromatosis, brain tumor, or both. |
| Q70341687 | Non-von Recklinghausen's neurofibromatosis presenting as hemifacial neurofibromas and contralateral café au lait spots |
| Q28291223 | Noonan syndrome with café‐au‐lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus |
| Q41767343 | Noonan's syndrome and neurofibromatosis |
| Q55738710 | Objective assessment of nasality in flemish adults with neurofibromatosis type 1 |
| Q43115107 | Obstructive jaundice secondary to ampullary adenocarcinoma in neurofibromatosis type 1. |
| Q34192974 | Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor |
| Q33581671 | Oncogene v-src transforms and establishes embryonic rodent fibroblasts but not diploid human fibroblasts |
| Q30503603 | Ophthalmic manifestations of neurofibromatosis |
| Q37039768 | Orbitotemporal neurofibromatosis: classification and treatment |
| Q42457291 | Palmar melanotic macules. A sign of neurofibromatosis |
| Q36425828 | Partial Blindness to Submicron Topography in NF1 Haploinsufficient Cultured Fibroblasts Indicates a New Function of Neurofibromin in Regulation of Mechanosensoric |
| Q54027004 | Pathological dislocation of the hip in neurofibromatosis: a case report. |
| Q30501233 | Penetrance of von Recklinghausen neurofibromatosis: a distinction between predecessors and descendants |
| Q33874531 | Perioperative management of children with congenital phakomatoses |
| Q36595387 | Peripheral retinal ischemia in a young Indian woman with neurofibromatosis type 1. |
| Q35185266 | Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17. |
| Q48371042 | Picosecond 532-nm neodymium-doped yttrium aluminium garnet laser-a novel and promising modality for the treatment of café-au-lait macules. |
| Q39603243 | Pigmentary abnormalities in genetic disorders. |
| Q49397207 | Plexiform Neurofibroma in the Axilla with Intraosseous Neurofibroma in the Humerus in Neurofibromatosis 5. |
| Q33645287 | Posterior mediastinal neurogenic tumors in infants and children |
| Q37391531 | Potential influences on mathematical difficulties in children and adolescents with neurofibromatosis, type 1. |
| Q70873052 | Precocious puberty, growth hormone deficiency, and neurofibromatosis |
| Q64042250 | Primary diffuse neurofibroma of the urinary bladder: a rare case report and review of the literature |
| Q40157328 | Primary melanocytic schwannoma of the stomach. Evidence of dual melanocytic and schwannian differentiation in an extra-axial site in a patient without neurofibromatosis |
| Q41917599 | Primary osteopathy of vertebrae in a neurofibromatosis type 1 murine model |
| Q36476833 | Progress toward the Isolation and Characterization of the Genes Causing Neurofibromatosis |
| Q48152921 | Proliferative activity as measured by MIB-1 labeling index and long-term outcome of visual pathway astrocytomas in children |
| Q72863373 | Protein-losing enteropathy caused by mesenteric vascular involvement of neurofibromatosis |
| Q64097213 | Pulmonary arterial hypertension: A rare yet fatal complication of Neurofibromatosis Type 1 |
| Q52864428 | Quantitative morphology of the corpus callosum in children with neurofibromatosis and attention-deficit hyperactivity disorder. |
| Q74436892 | Rare combination of spinal lesions and subcutaneous meningioma in a 44 year old man |
| Q40525105 | Ras signaling and NF1. |
| Q30495052 | Recent developments in the diagnosis and management of neurofibromatosis |
| Q36678858 | Recent insights into the molecular pathogenesis of pheochromocytoma and paraganglioma |
| Q53171094 | Recurrent rupture of intercostal artery aneurysms in neurofibromatosis type 1. |
| Q48276326 | Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): a follow-up study |
| Q53486122 | Renovascular hypertension associated with neurofibromatosis: a case report. |
| Q39193840 | Renovascular hypertension in neurofibromatosis |
| Q35860698 | Repression of the NF1 gene by Tax may expain the development of neurofibromas in human T-lymphotropic virus type 1 transgenic mice |
| Q39699379 | Role of ultrasonography in detection of renal artery pseudoaneurysm caused by retroperitoneal malignant peripheral nerve sheath tumor in a patient with neurofibromatosis type 1. |
| Q36271830 | Ruptured popliteal aneurysm resulting from neurofibromatosis-a case report and review of the literature |
| Q69961257 | Secondary hypertension and neurofibromatosis: bilateral renal artery stenosis and coarctation of the abdominal aorta |
| Q79736331 | Segmental neurofibromatosis |
| Q50101444 | Segmental neurofibromatosis |
| Q69195114 | Segmental neurofibromatosis |
| Q41641153 | Segmental neurofibromatosis: case reports and review |
| Q53675679 | Segmentally distributed neurofibromatosis associated with adenocarcinoma of the colon. |
| Q48447152 | Serum mitogenic activity on in vitro glial cells in Neurofibromatosis type 1. |
| Q34432977 | Small G Protein Signaling in Neuronal Plasticity and Memory Formation: The Specific Role of Ras Family Proteins |
| Q24806653 | Small bowel gastrointestinal stromal tumours and ampullary cancer in Type 1 neurofibromatosis |
| Q35359138 | Soft tissue sarcomas |
| Q41031295 | Soft tissue sarcomas: diagnosis, classification and prognostic factors |
| Q34213017 | Solid tumors associated with multiple endocrine neoplasias |
| Q42050055 | Specific expression of the neurofibromatosis type 1 gene (NF1) in the hamster Schwann cell |
| Q55480117 | Sporadic acute lymphocytic leukemia arising in a patient with neurofibromatosis and xanthogranulomatosis. |
| Q36781660 | Staged Management of a Ruptured Internal Mammary Artery Aneurysm |
| Q33889193 | Structural analysis of the GAP-related domain from neurofibromin and its implications |
| Q36265262 | Structural gene for beta-nerve growth factor not defective in familial dysautonomia |
| Q52091100 | Subarachnoid Hemorrhage Because of Distal Superior Cerebellar Artery Dissection in Neurofibromatosis Type 1. |
| Q70476030 | Submandibular and axillary schwannomas not associated with von Recklinghausen's disease |
| Q38162895 | Syndrome-associated soft tissue tumours |
| Q34089379 | T1 Breast Cancer Associated with Von Recklinghausen's Neurofibromatosis |
| Q49136405 | T2-weighted hyperintensities (unidentified bright objects) in children with neurofibromatosis 1: their impact on cognitive function |
| Q55483973 | TP53 Gene Mutations and 17p Deletions in Human Astrocytomas |
| Q39213212 | Testicular teratoma and peripheral neurofibromatosis |
| Q37796203 | The Diagnostic and Clinical Significance of Café-au-lait Macules |
| Q40111985 | The Ichthyoses-Pathogenesis and Prenatal Diagnosis: A Review of Recent Advances |
| Q24538135 | The Proteus syndrome: the Elephant Man diagnosed |
| Q33655914 | The diagnostic value of café-au-lait macules |
| Q59238605 | The expanded role of NF1 |
| Q38026811 | The genetic and environmental causes of pulmonary fibrosis |
| Q39478899 | The genodermatoses and their significance in pediatric dermatology. |
| Q24309158 | The protein product of the neurofibromatosis type 1 gene is expressed at highest abundance in neurons, Schwann cells, and oligodendrocytes |
| Q40273172 | The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections |
| Q30501214 | The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus |
| Q48121198 | Three-dimensional multivoxel proton MR spectroscopy of the brain in children with neurofibromatosis type 1. |
| Q35816885 | Transplacental induction of peripheral nervous tumor in the Syrian golden hamster by N-nitroso-N-ethylurea. A new animal model for von Recklinghausen's neurofibromatosis |
| Q74835996 | Tumor-related dysmotility: gastrointestinal dysmotility syndromes associated with tumors |
| Q28594951 | Tumour predisposition in mice heterozygous for a targeted mutation in Nf1 |
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