case report | Q2782326 |
scholarly article | Q13442814 |
P50 | author | Jerzy Roman Kowalczyk | Q21328387 |
Michał Korostyński | Q67880705 | ||
Kinga Kwiecinska | Q90964014 | ||
Marcin Piechota | Q96058271 | ||
Walentyna Balwierz | Q102361240 | ||
Szymon Skoczeń | Q125172866 | ||
Angelina Moryl-Bujakowska | Q125173024 | ||
Wojciech Młynarski | Q30903317 | ||
P2093 | author name string | Wojciech Strojny | |
Konrad Stepien | |||
Piotr Centkowski | |||
Elzbieta Wyrobek | |||
Magdalena Rej | |||
P2860 | cites work | Human papillomavirus infection in Netherton's syndrome | Q73895182 |
Cushing syndrome from percutaneous absorption of 1% hydrocortisone ointment in Netherton syndrome | Q79774717 | ||
Penile cancer in a man with netherton syndrome | Q40163272 | ||
Netherton's syndrome: a syndrome of elevated IgE and characteristic skin and hair findings | Q40570245 | ||
Netherton syndrome with multiple non-melanoma skin cancers | Q42436922 | ||
Significant absorption of topical tacrolimus in 3 patients with Netherton syndrome. | Q43639646 | ||
Impact of TRPV3 on the development of allergic dermatitis as a dendritic cell modulator | Q45381582 | ||
JAK2 aberrations in childhood B-cell precursor acute lymphoblastic leukemia | Q47095048 | ||
TRPV3 Channel in Keratinocytes in Scars with Post-Burn Pruritus | Q47096526 | ||
Considerations in surgical management of a Buschke-Lowenstein tumor in Netherton syndrome: A case report | Q47343035 | ||
The effects of R683S (G) genetic mutations on the JAK2 activity, structure and stability. | Q50925561 | ||
A preliminary study of new single polymorphisms in the T helper type 17 pathway for psoriasis in the Korean population. | Q51367413 | ||
Philadelphia Chromosome-like Acute Lymphoblastic Leukemia. | Q54989161 | ||
Infliximab Infusions for Netherton Syndrome: Sustained Clinical Improvement Correlates with a Reduction of Thymic Stromal Lymphopoietin Levels in the Skin | Q61843707 | ||
Genetic Profile and Clinical Implications of Hepatoblastoma and Neuroblastoma Coexistence in a Child | Q64076272 | ||
Genome instability syndromes caused by impaired DNA repair and aberrant DNA damage responses | Q64389645 | ||
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping. | Q24539101 | ||
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients | Q24643416 | ||
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome | Q28145552 | ||
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. | Q34126886 | ||
Outcomes of children with BCR-ABL1–like acute lymphoblastic leukemia treated with risk-directed therapy based on the levels of minimal residual disease | Q34172033 | ||
Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemia | Q34314927 | ||
6MP adherence in a multiracial cohort of children with acute lymphoblastic leukemia: a Children's Oncology Group study | Q34318474 | ||
Comèl-Netherton syndrome defined as primary immunodeficiency | Q34997608 | ||
A Patient with Congenital Ichthyosis Hystrix (Disseminated Congenital Naevus) and Acute Lymphoblastic Leukaemia | Q35105476 | ||
Olmsted syndrome: clinical, molecular and therapeutic aspects | Q35215730 | ||
Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry. | Q35909685 | ||
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015. | Q36319898 | ||
Hereditary cancer predisposition in children: genetic basis and clinical implications | Q36461758 | ||
Nonadherence to oral mercaptopurine and risk of relapse in Hispanic and non-Hispanic white children with acute lymphoblastic leukemia: a report from the children's oncology group | Q36695870 | ||
B-cell acute lymphoblastic leukemia associated with SET-NUP214 rearrangement: A case report and review of the literature | Q36740935 | ||
Genetic predispositions to childhood leukemia. | Q37073895 | ||
JAK mutations in high-risk childhood acute lymphoblastic leukemia | Q37224111 | ||
Malignant skin tumours in patients with inherited ichthyosis | Q37868636 | ||
Netherton syndrome: skin inflammation and allergy by loss of protease inhibition | Q38076305 | ||
TRPV3. | Q38206427 | ||
NUP214 fusion genes in acute leukemia (Review). | Q38239669 | ||
Netherton Syndrome: A Genotype-Phenotype Review | Q39025260 | ||
Ph-like acute lymphoblastic leukemia | Q39027852 | ||
Risk-adjusted therapy of acute lymphoblastic leukemia can decrease treatment burden and improve survival: treatment results of 2169 unselected pediatric and adolescent patients enrolled in the trial ALL-BFM 95. | Q39835436 | ||
Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation. | Q40006125 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P921 | main subject | Netherton syndrome | Q9390284 |
lymphoblastic leukemia | Q18553852 | ||
P304 | page(s) | 1477 | |
P577 | publication date | 2019-01-01 | |
P1433 | published in | Frontiers in Oncology | Q26839986 |
P1476 | title | Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence-First Report in the Literature | |
P478 | volume | 9 |
Q96954627 | Polymorphisms of SLC19A1 80 G>A, MTHFR 677 C>T, and Tandem TS Repeats Influence Pharmacokinetics, Acute Liver Toxicity, and Vomiting in Children With Acute Lymphoblastic Leukemia Treated With High Doses of Methotrexate | cites work | P2860 |
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