Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders. - Wikidata - wikimedia - TriplyDB

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

http://www.wikidata.org/entity/Q34543994

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French database of children and adolescents with Prader-Willi syndrome.Severe tooth wear in Prader-Willi syndrome. A case-control study.Nutritient intake of young children with Prader-Willi syndrome.Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome Different distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly.Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.Prader-Willi syndrome: A primer for clinicians.Deaths in children with Prader-Willi syndrome. A contribution to the debate about the safety of growth hormone treatment in children with PWS.Prader-Willi syndrome in neonates: twenty cases and review of the literature in Southern China.Endocrine problems in children with Prader-Willi syndrome: special review on associated genetic aspects and early growth hormone treatment.Death during GH therapy in children with Prader-Willi syndrome: description of two new cases.Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition Mortality in Prader-Willi syndrome.Prader-Willi syndrome: an update and review for the primary pediatrician.Neural correlates of self-injurious behavior in Prader-Willi syndrome Assessment of sleep and breathing in adults with prader-willi syndrome: a case control series Scoliosis in patients with Prader Willi Syndrome - comparisons of conservative and surgical treatment.Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding.A short clinical overview of Prader-Willi syndrome.A neuropsychological assessment of frontal cognitive functions in Prader-Willi syndrome.Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.Social/economic costs and health-related quality of life in patients with Prader-Willi syndrome in Europe.Long-term health outcomes in patients with Prader-Willi syndrome: a nationwide cohort study in Denmark.Ethnic and population differences in the genetic predisposition to human obesity.Adult Prader-Willi Syndrome: An Update on Management.Pituitary-Adrenal Axis in Prader Willi Syndrome.Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome: experience from a dedicated centre in France.Comparison of body composition, basal metabolic rate and metabolic outcomes of adults with Prader Willi syndrome or lesional hypothalamic disease, with primary obesity.Postprandial cardiac autonomic function in Prader-Willi syndrome.The impact of Prader-Willi syndrome on the family's quality of life and caregiving, and the unaffected siblings' psychosocial adjustment.On the origin of sensory impairment and altered pain perception in Prader-Willi syndrome: a neurophysiological study.Cardiac evaluation in children with Prader-Willi syndrome.Nutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype.Ghrelin level and weight loss after laparoscopic sleeve gastrectomy and gastric mini-bypass for Prader-Willi syndrome in Chinese.Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome.Social/economic costs and health-related quality of life in patients with rare diseases in Europe.Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.Rehabilitation priorities for individuals with Prader-Willi Syndrome.Characteristics of cardiac and vascular structure and function in Prader-Willi syndrome.Orofacial dysfunction in individuals with Prader-Willi syndrome assessed with NOT-S.

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P2860

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

http://www.wikidata.org/entity/Q34543994

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2004 nî lūn-bûn

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European Journal of Human Genetics

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Minimum prevalence, birth inci ...... der-Willi syndrome in Flanders

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Annick Vogels

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E Legius

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J P Fryns

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Jenneke Van Den Ende

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Koen Devriendt

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P2860

Prader-Willi syndrome

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

Birth prevalence of Prader-Willi syndrome in Australia.

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region.

Prevalence study of Prader-Willi syndrome in North Dakota.

Imprinting in Prader-Willi and Angelman syndromes.

Frequency of the Prader-Willi syndrome in the San-in district, Japan.

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