scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1051664771 |
P356 | DOI | 10.1007/S12519-014-0478-9 |
P698 | PubMed publication ID | 24801229 |
P5875 | ResearchGate publication ID | 262109797 |
P2093 | author name string | Alberto Verrotti | |
Salvatore Grosso | |||
Daniela Laino | |||
Claudia Soldani | |||
Renato d'Alonzo | |||
P2860 | cites work | Angelman syndrome: correlations between epilepsy phenotypes and genotypes | Q46360972 |
Pituitary height and neuroradiological alterations in patients with Prader-Labhart-Willi syndrome | Q47271631 | ||
MR of the pituitary in patients with Prader-Willi syndrome: size determination and imaging findings | Q47341518 | ||
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients | Q47397187 | ||
Imprinting in Prader-Willi and Angelman syndromes | Q48013064 | ||
Genomic organization of the UBE3A/E6-AP gene and related pseudogenes | Q48040390 | ||
Diagnosis of Angelman syndrome: clinical and EEG criteria | Q48158829 | ||
Brain developmental abnormalities in Prader-Willi syndrome detected by diffusion tensor imaging | Q48457273 | ||
Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome | Q48565179 | ||
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain | Q48630943 | ||
Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice | Q48661423 | ||
Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study | Q48663060 | ||
The origin of excessive daytime sleepiness in the Prader-Willi syndrome. | Q48858475 | ||
Epilepsy in Prader-Willi syndrome: clinical characteristics and correlation to genotype. | Q51668368 | ||
Prader-Willi syndrome. | Q51826464 | ||
Prader-Willi syndrome. | Q51886650 | ||
[MR imaging in mental retardation] | Q52036416 | ||
Prevalence of childhood epilepsy and distribution of epileptic syndromes: a population-based survey in Okayama, Japan. | Q53258891 | ||
Intracranial abnormalities detected by three-dimensional magnetic resonance imaging in Prader-Willi syndrome | Q56232697 | ||
Functional imprinting and epigenetic modification of the human SNRPN gene | Q72250009 | ||
Clinical report—health supervision for children with Prader-Willi syndrome | Q83039727 | ||
Characteristics and frequency of seizure disorder in 56 patients with Prader-Willi syndrome | Q84077723 | ||
Physical health problems in adults with Prader-Willi syndrome | Q84745173 | ||
Evaluating the frequency and characteristics of seizures in 142 Japanese patients with Prader-Willi syndrome | Q87041771 | ||
Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin | Q28585818 | ||
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis | Q31165084 | ||
Current management of febrile seizures in Japan: an overview | Q33512177 | ||
Angelman syndrome: a review of clinical and genetic aspects | Q33760683 | ||
Prader-Willi syndrome: consensus diagnostic criteria. | Q34061685 | ||
Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation | Q34388784 | ||
Imprinting-mutation mechanisms in Prader-Willi syndrome | Q34388796 | ||
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria | Q34428675 | ||
Epilepsy in children | Q34493734 | ||
A comprehensive team approach to the management of patients with Prader-Willi syndrome | Q35928285 | ||
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy. | Q36783665 | ||
Prader–Willi syndrome and Angelman syndrome | Q37783981 | ||
New onset epilepsy in Prader-Willi syndrome: semiology and literature review | Q37788402 | ||
Metabolic and endocrine effects of valproic acid chronic treatment | Q38146282 | ||
Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome | Q40641875 | ||
Investigation of thermoregulatory characteristics in patients with Prader-Willi syndrome | Q40704899 | ||
Cataplexy in the Prader-Willi syndrome | Q43100592 | ||
Multi-institutional study on the correlation between chromosomal abnormalities and epilepsy | Q44589437 | ||
Epilepsy in Prader-Willi syndrome: experience of a national referral centre | Q45211736 | ||
P433 | issue | 2 | |
P921 | main subject | Prader–Willi syndrome | Q594013 |
P304 | page(s) | 108-113 | |
P577 | publication date | 2014-05-07 | |
P1433 | published in | World Journal of Pediatrics | Q15763275 |
P1476 | title | Epilepsy in Prader-Willi syndrome: clinical, diagnostic and treatment aspects | |
P478 | volume | 10 |
Q38703279 | Clinical and Molecular Characterization of Prader-Willi Syndrome. | cites work | P2860 |
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