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 *

179 related articles for article (PubMed ID: 12757359)

  • 1. Two children with muscular dystrophies ascertained due to referral for diagnosis of autism.
    Zwaigenbaum L; Tarnopolsky M
    J Autism Dev Disord; 2003 Apr; 33(2):193-9. PubMed ID: 12757359
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Usefulness of test: manual muscle testing, goniometry, and daily activities for differential diagnosis of Duchenne muscular dystrophy, Becker's mild muscular dystrophy and Becker's severe muscular dystrophy.
    Alvarez M; Rodriguez I; Zuñiga-Charles MA
    Int J Rehabil Res; 1998 Mar; 21(1):79-85. PubMed ID: 9924669
    [No Abstract]   [Full Text] [Related]  

  • 3. Delayed diagnosis of Duchenne muscular dystrophy.
    Mohamed K; Appleton R; Nicolaides P
    Eur J Paediatr Neurol; 2000; 4(5):219-23. PubMed ID: 11030068
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Limb-girdle muscular dystrophy in MRI].
    Herzog H; Schröder RJ
    Rofo; 2003 Oct; 175(10):1432-4. PubMed ID: 14556115
    [No Abstract]   [Full Text] [Related]  

  • 5. Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies.
    Yis U; Baydan F; Karakaya M; Hız Kurul S; Cirak S
    Biomed Res Int; 2016; 2016():3128735. PubMed ID: 27123443
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Muscular dystrophies.
    Kalra V
    Indian J Pediatr; 2000 Dec; 67(12):923-8. PubMed ID: 11262992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Differential diagnosis of Becker and Duchenne muscular dystrophy].
    Alvarez Leal M; Hernández Sifuentes PM; Pérez-Zuno JA
    Gac Med Mex; 1994; 130(6):454-8. PubMed ID: 7557060
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Infantile autism and Duchenne muscular dystrophy.
    Komoto J; Usui S; Otsuki S; Terao A
    J Autism Dev Disord; 1984 Jun; 14(2):191-5. PubMed ID: 6746506
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identifying Non-Duchenne Muscular Dystrophy-Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs: A Review.
    Gatheridge MA; Kwon JM; Mendell JM; Scheuerbrandt G; Moat SJ; Eyskens F; Rockman-Greenberg C; Drousiotou A; Griggs RC
    JAMA Neurol; 2016 Jan; 73(1):111-6. PubMed ID: 26594870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The diagnosis of muscular dystrophy in patients referred for language delay.
    Kaplan LC; Osborne P; Elias E
    J Child Psychol Psychiatry; 1986 Jul; 27(4):545-9. PubMed ID: 3745353
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The muscular dystrophies.
    Seiler J; Bope ET
    Am Fam Physician; 1986 Jul; 34(1):123-8. PubMed ID: 3728255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Symptomatic carriers of muscular dystrophy.
    Azam M
    J Pak Med Assoc; 1997 Mar; 47(3):89-93. PubMed ID: 9131861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Interview - muscular dystrophies - worldwide search for patients].
    Walter M
    Z Orthop Unfall; 2011 Aug; 149(4):365-7. PubMed ID: 21845546
    [No Abstract]   [Full Text] [Related]  

  • 14. [Limb-girdle syndrome. A study of 46 cases].
    Ferrer X; Larrivière M; Coquet M; Ellie E; Lagueny A; Julien J
    Rev Neurol (Paris); 1993; 149(12):788-93. PubMed ID: 7997739
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detection.
    Percy ME; Chang LS; Murphy EG; Oss I; Verellen-Dumoulin C; Thompson MW
    Muscle Nerve; 1979; 2(5):329-39. PubMed ID: 492209
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chart validation of an algorithm for identifying hereditary progressive muscular dystrophy in healthcare claims.
    Chen X; Agiro A; Martin AS; Lucas AM; Haynes K
    BMC Med Res Methodol; 2019 Aug; 19(1):174. PubMed ID: 31399066
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy.
    North KN; Miller G; Iannaccone ST; Clemens PR; Chad DA; Bella I; Smith TW; Beggs AH; Specht LA
    Neurology; 1996 Feb; 46(2):461-5. PubMed ID: 8614513
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delayed language onset as a predictor of clinical symptoms in pervasive developmental disorders.
    Eisenmajer R; Prior M; Leekam S; Wing L; Ong B; Gould J; Welham M
    J Autism Dev Disord; 1998 Dec; 28(6):527-33. PubMed ID: 9932239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unusual Presentations of Dystrophinopathies in Childhood.
    Allen NM; Ewer A; Nakou V; Konstantoulaki E; Wraige E; Gowda V; Jungbluth H
    Pediatrics; 2018 Apr; 141(Suppl 5):S510-S514. PubMed ID: 29610182
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Incidental raised transaminases: a clue to muscle disease.
    Urganci N; Arapoğlu M; Serdaroğlu P; Nuhoğlu A
    Ann Trop Paediatr; 2006 Dec; 26(4):345-8. PubMed ID: 17132300
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.