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searching for Prader–Willi syndrome 26 found (191 total)

Microorchidism (127 words) [view diff] exact match in snippet view article find links to article

of other genetic disorders, including Klinefelter's Syndrome and Prader-Willi syndrome, as well as other multiple malformation disorders. The degree of

Cannabidivarin (457 words) [view diff] case mismatch in snippet view article find links to article

Phase-2 trials for adult epilepsy, for childhood epilepsy and for Prader-Willi Syndrome. List of investigational analgesics Turner CE, Cheng PC, Lewis GS

International System for Human Cytogenomic Nomenclature (408 words) [view diff] case mismatch in snippet view article find links to article

A tumour karyotype in a male with loss of the Y chromosome, (B) Prader–Willi Syndrome i.e. deletion in the 15q11-q12 region and (C) an arbitrary karyotype

George A. Bray (1,365 words) [view diff] case mismatch in snippet view article find links to article

obesity in patients with hypothalamic injury and in patients with the Prader-Willi Syndrome. After moving to the Pennington Center in 1989 Bray began research

PAR1 (gene) (436 words) [view diff] exact match in snippet view article

NE, et al. (1996). "Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint". Nat. Genet. 12 (4): 452–4. doi:10

Potassium ascorbate (305 words) [view diff] no match in snippet view article find links to article

effects of potassium ascorbate with ribose therapy in a case with Prader Willi Syndrome". Disease Markers. 33 (4): 179–183. doi:10.3233/DMA-2012-0922. ISSN 1875-8630

Nissim Benvenisty (1,672 words) [view diff] exact match in snippet view article find links to article

(such as Fragile X syndrome) and imprinting disorders (such as Prader-Willi syndrome). Tumorigenicity and immunogenicity of human pluripotent stem cells:

NIPA2 (410 words) [view diff] exact match in snippet view article find links to article

between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome". Pediatrics. 118 (4): e1276–e1283. doi:10.1542/peds.2006-0424.

TUBGCP5 (449 words) [view diff] exact match in snippet view article find links to article

between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader–Willi syndrome". Pediatrics. 118 (4): e1276–83. doi:10.1542/peds.2006-0424. PMC 5453799

NIPA1 (671 words) [view diff] exact match in snippet view article find links to article

between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome". Pediatrics. 118 (4): e1276–83. doi:10.1542/peds.2006-0424. PMC 5453799

Seiji Nishino (558 words) [view diff] exact match in snippet view article find links to article

deficient narcoleptic mice Decline of CSF orexin (hypocretin) levels in Prader-Willi syndrome A PERIOD3 variant causes a circadian phenotype and is associated

Estonian Chamber of People with Disabilities (622 words) [view diff] no match in snippet view article find links to article

diseases, EURORDIS, where the Chamber is represented by the Estonian Prader Willi Syndrome Association. The Chamber also shares its experiences with Georgia

CYFIP1 (921 words) [view diff] exact match in snippet view article find links to article

between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome". Pediatrics. 118 (4): e1276–83. doi:10.1542/peds.2006-0424. PMC 5453799

John Langdon Down (1,725 words) [view diff] exact match in snippet view article find links to article

research and was the first person to publish a description of the Prader-Willi syndrome, which he called 'polysarcia'. In 1887, he wrote a book entitled

HGH controversies (2,297 words) [view diff] exact match in snippet view article find links to article

and a handful of uncommon conditions like short bowel syndrome or Prader-Willi syndrome, a congenital disease that causes reduced muscle tone and a lack

Camping Unlimited: Camp Krem (501 words) [view diff] case mismatch in snippet view article find links to article

syndrome, intellectual disabilities, mobility limitations, and Prader-Willi Syndrome. One of the goals of Camp Krem is to provide "planned permissiveness

Chromosomal inversion (1,941 words) [view diff] case mismatch in snippet view article find links to article

A tumour karyotype in a male with loss of the Y chromosome, (B) Prader–Willi Syndrome i.e. deletion in the 15q11-q12 region and (C) an arbitrary karyotype

Neuroimmunology (2,794 words) [view diff] exact match in snippet view article find links to article

"Light optical precision measurements of the active and inactive Prader–Willi syndrome imprinted regions in human cell nuclei". Differentiation. 76 (1):

Greater Ottawa Kingfish Swim Club (1,141 words) [view diff] exact match in snippet view article find links to article

nationalpost.com. Retrieved 2016-02-04. "Paralympic hopeful with Prader-Willi syndrome finds salvation through swimming | Toronto Star". Thestar.com. 2012-03-30

Gait analysis (2,935 words) [view diff] exact match in snippet view article find links to article

Treatment improves gait pattern and posture in adult patients with Prader–Willi syndrome". International Journal of Osteopathic Medicine. 19: 35–43. doi:10

Nondisjunction (2,857 words) [view diff] exact match in snippet view article find links to article

disomy of chromosome 15 is, for example, seen in some cases of Prader-Willi syndrome and Angelman syndrome. Mosaicism syndromes can be caused by mitotic

HERC2 (3,353 words) [view diff] exact match in snippet view article find links to article

(1992). "The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito". Mammalian

Fluoxetine (11,815 words) [view diff] case mismatch in snippet view article find links to article

February 2024. Hagerman RJ (16 September 1999). "Angelman Syndrome and Prader-Willi Syndrome". Neurodevelopmental Disorders: Diagnosis and Treatment. Oxford

Philanthropy of Jolin Tsai (3,346 words) [view diff] case mismatch in snippet view article find links to article

Kong Peekaboo Project" charity sale, with all proceeds donated to Prader-Willi Syndrome Association Taiwan. In December 2017, Tsai was invited by Huashan

2003 Birthday Honours (14,994 words) [view diff] case mismatch in snippet view article find links to article

Reynolds. For services to People with Learning Difficulties and Prader-Willi Syndrome. Peter Robert Richardson, Teacher, Haycliffe Special School, Bradford

2020 Queen's Birthday Honours (Australia) (12,857 words) [view diff] case mismatch in snippet view article

Georgina Catherine Loughnan – For service to people living with Prader-Willi Syndrome. Dr John Allan Lowndes – For service to the law, and to the judiciary