101 related articles for article (PubMed ID: 27402947)
1. Clinical Reasoning: A tale of a hypotonic infant.
Al-Ghamdi F; Ghosh PS
Neurology; 2016 Jul; 87(2):e11-6. PubMed ID: 27402947
[No Abstract] [Full Text] [Related]
2. A hypotonic infant with tachycardia and fever of unknown origin.
Yalçin SS; Kale E; Topaloğlu H; Tunçbilek E
J Pediatr Health Care; 2007; 21(2):115-6, 136-8. PubMed ID: 17321911
[No Abstract] [Full Text] [Related]
3. [Prader-Willi syndrome in 22-year-old man--case study].
Kardas P; Adamiak-Kardas M
Wiad Lek; 2001; 54(11-12):709-14. PubMed ID: 11928560
[TBL] [Abstract][Full Text] [Related]
4. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome].
Witkowski R; Ullrich E; Pietsch P; Weber K; Heller K; Losanowa T; Nitz I
Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109
[TBL] [Abstract][Full Text] [Related]
5. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ
Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122
[TBL] [Abstract][Full Text] [Related]
6. Laryngeal clefts in Prader-Willi syndrome: Feeding difficulties and aspiration not always caused by hypotonia.
Rodrigo ML; Heubi C; Chiou E; Scheimann A
Am J Med Genet A; 2024 Aug; 194(8):e63634. PubMed ID: 38619072
[TBL] [Abstract][Full Text] [Related]
7. A 3 year old with obesity and hypotonia. Prader-Willi syndrome.
Charrow J
Pediatr Ann; 2007 May; 36(5):284-6. PubMed ID: 17515168
[No Abstract] [Full Text] [Related]
8. Distal arthrogryposis and neonatal hypotonia: an unusual presentation of Prader-Willi syndrome (PWS).
Denizot S; Boscher C; Le Vaillant C; Rozé JC; Gras Le Guen C
J Perinatol; 2004 Nov; 24(11):733-4. PubMed ID: 15510104
[TBL] [Abstract][Full Text] [Related]
9. A 5-month-old boy with delay in growth and development and decreased muscle tone.
Hucthagowder V; Shinawi M; Lockwood CM
Clin Chem; 2015 Jan; 61(1):50-4. PubMed ID: 25550475
[No Abstract] [Full Text] [Related]
10. [Neonatal hypotonia in Prader-Willi syndrome due to t(15;16)].
Fernández-Novoa MC; Vargas MT; Santano MR; Moya J; Garnacho MC
Rev Neurol; 2000 Sep 1-15; 31(5):499-500. PubMed ID: 11027108
[No Abstract] [Full Text] [Related]
11. Prevalence of Prader-Willi syndrome among infants with hypotonia.
Tuysuz B; Kartal N; Erener-Ercan T; Guclu-Geyik F; Vural M; Perk Y; Erçal D; Erginel-Unaltuna N
J Pediatr; 2014 May; 164(5):1064-7. PubMed ID: 24582009
[TBL] [Abstract][Full Text] [Related]
12. Early diagnosis of Prader-Willi syndrome in a newborn.
Chen CJ; Hsu ML; Yuh YS; Cheng SN; Kuo PL; Lee CM
Acta Paediatr Taiwan; 2004; 45(2):108-10. PubMed ID: 15335123
[TBL] [Abstract][Full Text] [Related]
13. Polyhydramnios associated with Prader-Willi syndrome.
Akiba Y; Ono M; Shirahashi M; Noda S; Nishijima S; Amagata T; Kusano R; Fuke T; Hayashida S; Ikeda T; Yakubo K; Fukuiya T
J Obstet Gynaecol; 2015; 35(7):752-3. PubMed ID: 26291428
[No Abstract] [Full Text] [Related]
14. The high frequency of genetic diseases in hypotonic infants referred by neuropediatrics.
Vilchis Z; Najera N; Pérez-Duran J; Najera Z; Gonzalez L; del Refugio Rivera M; Queipo G
Am J Med Genet A; 2014 Jul; 164A(7):1702-5. PubMed ID: 24715477
[TBL] [Abstract][Full Text] [Related]
15. Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
Giurgiutiu DV; Espinoza LM; Wood TC; DuPont BR; Holden KR
J Child Neurol; 2008 Jan; 23(1):112-7. PubMed ID: 18184946
[TBL] [Abstract][Full Text] [Related]
16. Case 1: Hypotonia and Failure to Thrive in a 3-month-old Boy.
Weeks MJ; Vogt K; Kimball-Eayrs C
Pediatr Rev; 2016 Jan; 37(1):39-41. PubMed ID: 26729781
[No Abstract] [Full Text] [Related]
17. [Hypothalamus and behavior: the model Prader-Willi syndrome].
Tauber M
Rev Prat; 2015 Dec; 65(10):1273-4. PubMed ID: 26979019
[No Abstract] [Full Text] [Related]
18. Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia.
Ahn H; Seo GH; Oh A; Lee Y; Keum C; Heo SH; Kim T; Choi J; Kim GH; Ko TS; Yum MS; Lee BH; Choi IH
Medicine (Baltimore); 2020 Dec; 99(51):e23864. PubMed ID: 33371171
[TBL] [Abstract][Full Text] [Related]
19. Prader-Willi syndrome in a girl with 47,XX + mar karyotype.
Tomaszewska H; Lech H; Parcheta B; Piontek E; Wiśniewski L
Klin Padiatr; 1982; 194(5):328-31. PubMed ID: 7144051
[No Abstract] [Full Text] [Related]
20. [The syndrome of Prader-Willi (A case report)].
Drissi Touzani K; Marrakchi M; Chraibi F; Abdellaoui M; Benatiya Andaloussi I; Tahiri H
J Fr Ophtalmol; 2018 Apr; 41(4):e165-e166. PubMed ID: 29685739
[No Abstract] [Full Text] [Related]
[Next] [New Search]