BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 6.