Results 111 to 120 of about 15,656 (183)

Spectrum of genetic forms of obesity and related disorders: Prader-Willi-like syndromes (part 1)

Ожирение и метаболизм
Prader–Willi–like syndromes (PWLS) represent a heterogeneous group of disorders characterized by a set of key clinical features, including muscular hypotonia, obesity, psychomotor and speech developmental delay, and behavioral problems, in the absence of
E. G. Panchenko, E. P. Atavina-Ermakova, A. F. Nikolaeva, T. V. Boyko, O. V. Vasyukova, D. A. Kopytina, N. G. Mokrysheva, S. I. Kutsev   +7 more
doaj   +1 more source

A genetic condition that spans both extremes of the nutritional spectrum

Practical Laboratory Medicine
Prader-Willi syndrome (PWS) is a complex genetic disorder caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region, known as the Prader Willi critical region.
Lisa M. Johnson
doaj   +1 more source

Behaviour management in Prader-Willi syndrome [PDF]

, 1999
SIGLEAvailable from British Library Document Supply Centre-DSC:m00/17545 / BLDSC - British Library Document Supply CentreGBUnited ...
Prader-Willi Syndrome Association (UK) (United Kingdom)
core  

Endocrine management of children with Prader–Willi syndrome [PDF]

, 2013
Clarice Borschiver Medeiros,1 Ana Paula Bordallo,1 Flavio Moutinho Souza,2 Paulo Ferrez Collett-Solberg1,31Endocrinology Unit, Departamento de Medicina Interna, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro (UERJ ...
Medeiros CB, Souza FM, Bordallo AP, Collett-Solberg PF   +3 more
core  

Vortioxetine-Lurasidone Augmentation for Compulsive Scratching Behavior in Prader-Willi Syndrome: A Case Report. [PDF]

Neuropsychopharmacol Rep
Nagoshi Y.
europepmc   +1 more source

Growth Hormone-Induced Stridor in a Patient With Prader-Willi Syndrome. [PDF]

Clin Case Rep
Saad AM, Zaki H, Menon A, Hausdorff M, Manzi B.   +4 more
europepmc   +1 more source

Methylphenidate use in hyperphagic Prader-Willi syndrome: A clinical note. [PDF]

Indian J Psychiatry
Saruhan K.
europepmc   +1 more source

Diagnostic Utility of Muscle Ultrasound for Sarcopenia in Prader-Willi Syndrome: A Cross-Sectional Study. [PDF]

J Cachexia Sarcopenia Muscle
Yu LH, Wu HC, Tzeng IS, Luo YT, Tsai LP, Chiu V.   +5 more
europepmc   +1 more source

Aberrant local and global neural activation patterns in pediatric Prader-Willi syndrome. [PDF]

Front Neurosci
Liu J, Huang Z, Cai J, Zhu M, Peng S, Ding S, Wang L, Tang W, Sun C, Su J.   +9 more
europepmc   +1 more source

Severe respiratory complications in late-diagnosed Prader-Willi syndrome: a case report. [PDF]

J Med Case Rep
Tiwari SK, Joshi P, Mishra NR, Sonowal R, Bhunia NS.   +4 more
europepmc   +1 more source