The Prader-Willi syndrome

scientific article

The Prader-Willi syndrome is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1136/ADC.70.1.58
P932PMC publication ID1029686
P698PubMed publication ID8110011
P5875ResearchGate publication ID15089263

P2093author name stringWilson A
Donaldson MD
Stephenson JB
Cooke A
Greene SA
Chu CE
P2860cites workSmall nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical regionQ28208127
Genomic imprinting: review and relevance to human diseases.Q30501672
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisQ31165084
Precocious puberty in a male with Prader-Labhart-Willi syndromeQ70519795
The Prader-Willi syndromeQ71278557
Prader-Willi syndrome: neonatal presentation and later developmentQ71436966
Endocrine function in the Prader-Willi syndromeQ71503870
The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literatureQ33586909
An anthropometric study of 38 individuals with Prader-Labhart-Willi syndromeQ33828442
Prader-Willi syndrome: current understanding of cause and diagnosisQ33858951
Prader-Willi syndrome: consensus diagnostic criteria.Q34061685
FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regionsQ34356063
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionQ34461093
Physical features of Prader-Willi syndrome in neonatesQ34636505
Deletions of chromosome 15 as a cause of the Prader-Willi syndromeQ34718526
Prader-Willi Syndrome after age 15 yearsQ35114940
Occupational hydrocarbon exposure among fathers of Prader-Willi syndrome patients with and without deletions of 15q.Q35248500
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndromeQ35611528
Fenfluramine in Prader-Willi syndrome: a double blind, placebo controlled trialQ35625284
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.Q36783665
The Prader-Labhart-Willi syndrome: review of the literature and report of nine casesQ40065565
DNA deletion and its parental origin in Angelman syndrome patientsQ41135500
Beta-endorphin immunoreactivity in the plasma of patients with the Prader-Labhart-Willi syndrome and their normal siblingsQ41556526
Prader-Willi syndrome in siblings, due to unbalanced translocation between chromosomes 15 and 22.Q41790276
Weight control of children with Prader-Willi syndromeQ44413279
Linear growth response to exogenous growth hormone in Prader-Willi syndrome.Q45084955
Immunoreactive insulin and growth hormone responses in patients with Prader-Willi syndromeQ47974200
Anterior Pituitary Function in the Prader-Labhart-Willi (PLW) SyndromeQ48499530
The speech and language characteristics of children with Prader-Willi syndrome.Q50551149
The effects of naltrexone, an oral beta-endorphin antagonist, in children with the Prader-Willi syndrome.Q51206919
Plasma immunoreactive beta-melanocyte stimulating hormone (lipotropin) levels in individuals with Prader-Labhart-Willi syndrome.Q51627675
A reduced number of insulin receptors in patients with Prader-Willi syndromeQ51645463
Metabolic aspects of a protein-sparing modified fast in the dietary management of Prader-Willi obesityQ51667628
Emotional symptoms in Prader-Willi syndrome adolescents.Q52583296
Adults with Prader-Willi syndrome: abnormalities of sleep and behaviour.Q55311630
Gastric bypass for morbid obesity in children and adolescentsQ66913734
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expressionQ67510275
Neonatal Presentation of Prader-Willi SyndromeQ67735614
Out-patient dietary management in the Prader-Willi syndromeQ67757944
Food and children with Prader-Willi syndromeQ67829369
Standards for selected anthropometric measurements in Prader-Willi syndromeQ67979069
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13Q67993243
A nutrition survey of and recommendations for individuals with Prader-Willi syndrome who live in group homesQ68195829
Energy expenditure and body composition in Prader-Willi syndromeQ68260755
Molecular study of the Prader-Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patientsQ68324405
Growth hormone secretion in Prader-Willi syndromeQ68644237
Adults with Prader-Willi syndrome: a survey of 232 casesQ69022332
Familial Prader-Willi syndrome with apparently normal chromosomesQ69437089
Recurrence risk in Prader-Willi syndromeQ69437094
Paternal hydrocarbon exposure in Prader-Willi syndromeQ69911063
Evidence against growth hormone-releasing factor deficiency in children with idiopathic obesityQ70310886
P433issue1
P407language of work or nameEnglishQ1860
P304page(s)58-63
P577publication date1994-01-01
P1433published inArchives of Disease in ChildhoodQ4787296
P1476titleThe Prader-Willi syndrome
P478volume70

Reverse relations

cites work (P2860)
Q80520026Anthropometric and intellectual evaluation of individuals with Prader-Willi syndrome
Q57905283Bilateral non-communicating paraurethral meatus in Prader-Willi syndrome
Q33721923Childhood leukaemia: a model of pre-obesity.
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Q35800882Clinical implications of gait analysis in the rehabilitation of adult patients with "Prader-Willi" Syndrome: a cross-sectional comparative study ("Prader-Willi" Syndrome vs matched obese patients and healthy subjects)
Q34796000Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes
Q72318701Diagnosing Prader-Willi syndrome
Q33625228Diagnosis in Prader-Willi syndrome
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Q57162083Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13
Q48868755GH secretion in Prader-Labhard-Willi syndrome: somatotrope responsiveness to GHRH is enhanced by arginine but not by pyridostigmine
Q38312497GH/IGF-I axis in Prader-Willi syndrome: evaluation of IGF-I levels and of the somatotroph responsiveness to various provocative stimuli. Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and Diabetology
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Q38299914Impairment of GH responsiveness to GH-releasing hexapeptide (GHRP-6) in Prader-Willi syndrome
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Q51987714Troglitazone ameliorates insulin resistance in a diabetic patient with Prader-Willi syndrome.
Q41167741Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
Q77366010[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling]

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