Results 171 to 180 of about 15,704 (225)
Fiber Intervention Study in Prader-Willi Syndrome: Insights into Metabolic and Microbiota Shifts.
J Clin Endocrinol MetabTan Q +14 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
The Lancet, 1968
IN 1956 Prader et al1first reported nine cases of a new syndrome. The symptom complex evolves to its full expression over a number of years. The prenatal course is usually uneventful, except for decreased fetal activity. Infants are born at term with a low birth weight.
J, Landwirth, A H, Schwartz, J A, Grunt
openaire +4 more sources
IN 1956 Prader et al1first reported nine cases of a new syndrome. The symptom complex evolves to its full expression over a number of years. The prenatal course is usually uneventful, except for decreased fetal activity. Infants are born at term with a low birth weight.
J, Landwirth, A H, Schwartz, J A, Grunt
openaire +4 more sources
Journal of Intellectual Disability Research, 1967
รปแสดง การเกด Deletion ของต าแหนง 15q11-13 โครโมโซมทก าหนดวาเปน P เปนโครโมโซมทไดมา จากพอ (paternal) และโครโมโซมทก าหนดวาเปน M คอโครโมโซมแทงทไดมาจากแม (maternal) จะเหนไดวา หากมการขาดหายไปของบรเวณ 15q11-13 ของโครโมโซมแทงทไดมาจากพอ จะท าใหเกด โรค Prader-Willi Syndrome แตหากเปนโครโมโซมแทงทไดมาจากแม จะท าใหเกด โรค Angelman Syndrome แสดงวาบรเวณ 15q11-13 ...
J, Juul, A, Dupont
openaire +4 more sources
รปแสดง การเกด Deletion ของต าแหนง 15q11-13 โครโมโซมทก าหนดวาเปน P เปนโครโมโซมทไดมา จากพอ (paternal) และโครโมโซมทก าหนดวาเปน M คอโครโมโซมแทงทไดมาจากแม (maternal) จะเหนไดวา หากมการขาดหายไปของบรเวณ 15q11-13 ของโครโมโซมแทงทไดมาจากพอ จะท าใหเกด โรค Prader-Willi Syndrome แตหากเปนโครโมโซมแทงทไดมาจากแม จะท าใหเกด โรค Angelman Syndrome แสดงวาบรเวณ 15q11-13 ...
J, Juul, A, Dupont
openaire +4 more sources
Journal of Obstetric, Gynecologic & Neonatal Nursing, 1989
Prader-Willi Syndrome (PWS) is a relatively common complex genetic disorder that is diagnostically and therapeutically challenging to health-care professionals. Nursing observations of significant neonatal feeding problems may assist in identification of the infant with PWS.
S B, Cassidy, D H, Ledbetter
openaire +4 more sources
Prader-Willi Syndrome (PWS) is a relatively common complex genetic disorder that is diagnostically and therapeutically challenging to health-care professionals. Nursing observations of significant neonatal feeding problems may assist in identification of the infant with PWS.
S B, Cassidy, D H, Ledbetter
openaire +4 more sources
Archives of Pediatrics & Adolescent Medicine, 1969
IN 1956, Prader et al1described a syndrome characterized by mental retardation, muscular hypotonia, obesity, short stature, and hypogonadism. In 1961, Prader and Willi2noted a marked tendency to develop diabetes mellitus. Forssman and Hagberg3observed that acromicria was such a constant feature that it should be considered characteristic of the ...
M M, Cohen, R J, Gorlin
openaire +2 more sources
IN 1956, Prader et al1described a syndrome characterized by mental retardation, muscular hypotonia, obesity, short stature, and hypogonadism. In 1961, Prader and Willi2noted a marked tendency to develop diabetes mellitus. Forssman and Hagberg3observed that acromicria was such a constant feature that it should be considered characteristic of the ...
M M, Cohen, R J, Gorlin
openaire +2 more sources
JAMA: The Journal of the American Medical Association, 1984
To the Editor.— Dr Wett's 1 article in A PIECE OF MY MIND did it to my peace of mind. Delay of recognizing the Prader-Willi (PW) syndrome occurs ever so often. The average age when PW syndrome is diagnosed in boys is close to 10 years and older than 10 years in girls. Many cases remain undiagnosed, notably in girls.
openaire +2 more sources
To the Editor.— Dr Wett's 1 article in A PIECE OF MY MIND did it to my peace of mind. Delay of recognizing the Prader-Willi (PW) syndrome occurs ever so often. The average age when PW syndrome is diagnosed in boys is close to 10 years and older than 10 years in girls. Many cases remain undiagnosed, notably in girls.
openaire +2 more sources
Lymphedema in Prader–Willi syndrome
International Journal of Dermatology, 2008AbstractA 20‐year‐old woman with Prader–Willi syndrome presented with heaviness and swelling in the lower legs and feet, which had developed after a fall. Lymphoscintigraphy showed a disturbed lymphatic drainage pattern in both lower extremities. Based on the clinical findings and the results of lymphoscintigraphic examination we made the diagnosis of ...
Martijn V, Heitink +5 more
openaire +2 more sources
Sleep in the Prader-Willi Syndrome
Archives of Neurology, 1985To the Editor. —Dr Vela-Bueno and colleagues 1 suggest that their finding of sleep-onset rapid-eye movement periods (SOREMPs) in the nocturnal sleep in five of nine patients with Prader-Willi syndrome (PWS) was due to hypothalamic dysfunction. They failed to mention that a shortened REM sleep latency could result from chronic REM sleep deprivation due
A J, Spielman, M J, Thorpy, A, Sher
openaire +2 more sources
Health Supervision for Children With Prader-Willi Syndrome [PDF]
Pediatrics, 2011 This set of guidelines was designed to assist the pediatrician in caring for children with Prader-Willi syndrome diagnosed by clinical features and confirmed by molecular testing. Prader-Willi syndrome provides an excellent example of how early diagnosis
null null, Shawn E. McCandless
exaly +2 more sources
Prader–Willi syndrome: an update
Current Opinion in Pulmonary Medicine, 2023Purpose of review Sleep disorders in Prader–Willi syndrome (PWS) range from respiratory to neurological disorders of sleep. We now recognize the role of excessive daytime sleepiness (present in the infant period and throughout life), and a modified narcolepsy phenotype with or without cataplexy.
openaire +2 more sources