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: 22480491)

  • 1. Relative frequency of congenital muscular dystrophy subtypes: analysis of the UK diagnostic service 2001-2008.
    Clement EM; Feng L; Mein R; Sewry CA; Robb SA; Manzur AY; Mercuri E; Godfrey C; Cullup T; Abbs S; Muntoni F
    Neuromuscul Disord; 2012 Jun; 22(6):522-7. PubMed ID: 22480491
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder].
    Castro-Gago M; Novo-Rodríguez MI; Pintos-Martínez E; Alonso-Martín A; Morales-Redondo R; Eirís-Puñal J
    Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital myopathies and muscular dystrophies.
    Gilbreath HR; Castro D; Iannaccone ST
    Neurol Clin; 2014 Aug; 32(3):689-703, viii. PubMed ID: 25037085
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A large series of immunohistochemically confirmed cases of congenital muscular dystrophy seen over a period of one decade.
    Nagappa M; Atchayaram N; Narayanappa G
    Neurol India; 2013; 61(5):481-7. PubMed ID: 24262449
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression].
    Xiong H; Yao S; Yuan Y; Chang XZ; Wu Y; Bao XH; Zhang YH; Wu HS; Chen L; Qin J; Wu XR
    Zhonghua Er Ke Za Zhi; 2006 Dec; 44(12):918-23. PubMed ID: 17254461
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period.
    Sframeli M; Sarkozy A; Bertoli M; Astrea G; Hudson J; Scoto M; Mein R; Yau M; Phadke R; Feng L; Sewry C; Fen ANS; Longman C; McCullagh G; Straub V; Robb S; Manzur A; Bushby K; Muntoni F
    Neuromuscul Disord; 2017 Sep; 27(9):793-803. PubMed ID: 28688748
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy.
    Sewry CA; D'Alessandro M; Wilson LA; Sorokin LM; Naom I; Bruno S; Ferlini A; Dubowitz V; Muntoni F
    Neuropediatrics; 1997 Aug; 28(4):217-22. PubMed ID: 9309712
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnosis and etiology of congenital muscular dystrophy.
    Peat RA; Smith JM; Compton AG; Baker NL; Pace RA; Burkin DJ; Kaufman SJ; Lamandé SR; North KN
    Neurology; 2008 Jul; 71(5):312-21. PubMed ID: 18160674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnosis and etiology of congenital muscular dystrophy: We are halfway there.
    O'Grady GL; Lek M; Lamande SR; Waddell L; Oates EC; Punetha J; Ghaoui R; Sandaradura SA; Best H; Kaur S; Davis M; Laing NG; Muntoni F; Hoffman E; MacArthur DG; Clarke NF; Cooper S; North K
    Ann Neurol; 2016 Jul; 80(1):101-11. PubMed ID: 27159402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Differential diagnosis of congenital muscular dystrophies.
    Klein A; Clement E; Mercuri E; Muntoni F
    Eur J Paediatr Neurol; 2008 Sep; 12(5):371-7. PubMed ID: 18588847
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital Muscular Dystrophy and Congenital Myopathy.
    Butterfield RJ
    Continuum (Minneap Minn); 2019 Dec; 25(6):1640-1661. PubMed ID: 31794464
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P
    Rev Neurol; 1999 Jan 16-31; 28(2):141-9. PubMed ID: 10101782
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy.
    Bendixen RM; Butrum J; Jain MS; Parks R; Hodsdon B; Nichols C; Hsia M; Nelson L; Keller KC; McGuire M; Elliott JS; Linton MM; Arveson IC; Tounkara F; Vasavada R; Harnett E; Punjabi M; Donkervoort S; Dastgir J; Leach ME; Rutkowski A; Waite M; Collins J; Bönnemann CG; Meilleur KG
    Neuromuscul Disord; 2017 Mar; 27(3):278-285. PubMed ID: 28087121
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?
    Mercuri E; Sewry CA; Brown SC; Brockington M; Jungbluth H; DeVile C; Counsell S; Manzur A; Muntoni F
    Neuropediatrics; 2000 Aug; 31(4):186-9. PubMed ID: 11071142
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
    Vainzof M; Marie SK; Reed UC; Schwartzman JS; Pavanello RC; Passos-Bueno MR; Zatz M
    Neuropediatrics; 1995 Dec; 26(6):293-7. PubMed ID: 8719743
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Merosin-deficient congenital muscular dystrophy type 1A.
    Buteică E; Roşulescu E; Burada F; Stănoiu B; Zăvăleanu M
    Rom J Morphol Embryol; 2008; 49(2):229-33. PubMed ID: 18516331
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Merosin-positive congenital muscular dystrophy: a large inbred family.
    Mahjneh I; Bushby K; Anderson L; Muntoni F; Tolvanen-Mahjneh H; Bashir R; Pizzi A; Brockington M; Marconi G
    Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brain MRI features of merosin-negative congenital muscular dystrophy.
    Ibrahim Abdulla JK; Vattoth S; Al Tawari AA; Pandey T; Abubacker S
    Australas Radiol; 2007 Dec; 51 Suppl():B221-3. PubMed ID: 17991069
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A unique case of congenital muscular dystrophy].
    Hermanová M; Vondrácek P; Lukás Z
    Cesk Patol; 2004 Apr; 40(2):57-62. PubMed ID: 15233018
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families.
    Safwat S; Flannery KP; El Beheiry AA; Mokhtar MM; Abdalla E; Manzini MC
    Neurogenetics; 2024 Apr; 25(2):93-102. PubMed ID: 38296890
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.