These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 38333661)

  • 1. A couple of the first cousins born with hypotonia and maternal polyhydramnios.
    Ahmadpour-Kacho M; Pasha YZ; Pournajaf S
    Clin Case Rep; 2024 Feb; 12(2):e8503. PubMed ID: 38333661
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical characteristics of pregnancies complicated by congenital myotonic dystrophy.
    Yee C; Choi SJ; Oh SY; Ki CS; Roh CR; Kim JH
    Obstet Gynecol Sci; 2017 Jul; 60(4):323-328. PubMed ID: 28791262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Congenital myotonic dystrophy--the significance of a handshake].
    Termote JU; Beemer FA; Wittebol-Post D; de Vries LS
    Ned Tijdschr Geneeskd; 2006 Jan; 150(2):65-70. PubMed ID: 16440558
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic Dystrophy.
    Zapata-Aldana E; Ceballos-Sáenz D; Hicks R; Campbell C
    J Neuromuscul Dis; 2018; 5(3):331-340. PubMed ID: 30010141
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Myotonic dystrophy is a significant cause of idiopathic polyhydramnios.
    Esplin MS; Hallam S; Farrington PF; Nelson L; Byrne J; Ward K
    Am J Obstet Gynecol; 1998 Oct; 179(4):974-7. PubMed ID: 9790382
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital Myotonic Dystrophy and Brugada Syndrome: A Report of Two Cases.
    Gupta K; Kennelly MR; Siddappa AM
    Am J Case Rep; 2020 Jan; 21():e919867. PubMed ID: 31915326
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital myotonic dystrophy: prenatal ultrasound findings and pregnancy outcome.
    Zaki M; Boyd PA; Impey L; Roberts A; Chamberlain P
    Ultrasound Obstet Gynecol; 2007 Mar; 29(3):284-8. PubMed ID: 17238150
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Steinert's disease and pregnancy. A case report and recent literature].
    Delest A; Elhage A; Cosson M; Leclercq G; Gremillet C; Pasquier F; Manouvrier-Hanu S; Decocq J; Delahousse G
    J Gynecol Obstet Biol Reprod (Paris); 1995; 24(2):177-80. PubMed ID: 7782590
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A neonatal case of congenital myotonic dystrophy].
    Ghizzi C; Cavalli C; Benedetti M; Bolognani M; Biban P
    Acta Biomed Ateneo Parmense; 2000; 71 Suppl 1():759-63. PubMed ID: 11424842
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.
    Zeesman S; Carson N; Whelan DT
    Am J Med Genet; 2002 Jan; 107(3):222-6. PubMed ID: 11807903
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Polyhydramnios in congenital myotonic dystrophy].
    Wieacker P; Wilhelm C; Fürste H; Schillinger H
    Z Geburtshilfe Perinatol; 1988; 192(1):36-7. PubMed ID: 3285617
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The utility of the determination of CTG trinucleotide repeat length in hypotonic infants.
    Bodensteiner JB; Byler DL; Jaynes ME
    Semin Pediatr Neurol; 1999 Sep; 6(3):243-5; discussion 245-6. PubMed ID: 10522348
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impact of prematurity and the CTG repeat length on outcomes in congenital myotonic dystrophy.
    Saito Y; Matsumura K; Kageyama M; Kato Y; Ohta E; Sumi K; Futatani T; Yoshida T
    BMC Res Notes; 2020 Jul; 13(1):350. PubMed ID: 32703309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Dystrophia myotonica and pregnancy].
    van de Biezenbos JB; Nijhuis JG; Brunner HG
    Ned Tijdschr Geneeskd; 1992 Dec; 136(50):2480-2. PubMed ID: 1465172
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital myotonic dystrophy; a report on thirteen cases and a review of the literature.
    Hageman AT; Gabreëls FJ; Liem KD; Renkawek K; Boon JM
    J Neurol Sci; 1993 Mar; 115(1):95-101. PubMed ID: 8166775
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Neonatal hypotonia of muscular origin: analysis of 50 cases].
    Floriach-Robert M; Cabello A; Simón De Las Heras R; Mateos Beato F
    Neurologia; 2001; 16(6):245-53. PubMed ID: 11423041
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital myotonic dystrophy in Britain. I. Clinical aspects.
    Harper PS
    Arch Dis Child; 1975 Jul; 50(7):505-13. PubMed ID: 1101835
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [DNA diagnosis in myotonic dystrophy].
    Tachi N
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital myotonic dystrophy.
    Gulati S; Kabra M; Gera S; Kalra V; Saxena R; Verma IC
    Indian J Pediatr; 2001 May; 68(5):451-3. PubMed ID: 11407162
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical effects of myotonic dystrophy on pregnancy and the neonate.
    Sarnat HB; O'Connor T; Byrne PA
    Arch Neurol; 1976 Jul; 33(7):459-65. PubMed ID: 779728
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.