BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 35725460)

  • 1. Dysferlinopathy misdiagnosed with juvenile polymyositis in the pre-symptomatic stage of hyperCKemia: a case report and literature review.
    Contreras-Cubas C; Barajas-Olmos F; Frayre-Martínez MI; Siordia-Reyes G; Guízar-Sánchez CC; García-Ortiz H; Orozco L; Baca V
    BMC Med Genomics; 2022 Jun; 15(1):139. PubMed ID: 35725460
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.
    Nguyen K; Bassez G; Krahn M; Bernard R; Laforêt P; Labelle V; Urtizberea JA; Figarella-Branger D; Romero N; Attarian S; Leturcq F; Pouget J; Lévy N; Eymard B
    Arch Neurol; 2007 Aug; 64(8):1176-82. PubMed ID: 17698709
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ["Therapy-resistant polymyositis" - is the diagnosis correct?].
    Ceccon G; Lehmann HC; Neuen-Jacob E; Meng G; Fink GR; Wunderlich G
    Z Rheumatol; 2017 Sep; 76(7):640-643. PubMed ID: 28523511
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Limb-girdle muscular dystrophy type 2B misdiagnosed as polymyositis at the early stage: Case report and literature review.
    Xu C; Chen J; Zhang Y; Li J
    Medicine (Baltimore); 2018 May; 97(21):e10539. PubMed ID: 29794729
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The clinical, myopathological, and molecular characteristics of 26 Chinese patients with dysferlinopathy: a high proportion of misdiagnosis and novel variants.
    Wang N; Han X; Hao S; Han J; Zhou X; Sun S; Tang J; Lu Y; Wu H; Ma S; Song X; Ji G
    BMC Neurol; 2022 Nov; 22(1):398. PubMed ID: 36319958
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recurrent, non-traumatic, non-exertional rhabdomyolysis after immunologic stimuli in a healthy adolescent female: a case report.
    Katz J; Labilloy A; Lee A
    BMC Pediatr; 2022 Aug; 22(1):515. PubMed ID: 36042458
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heterogeneous characteristics of Korean patients with dysferlinopathy.
    Park HJ; Hong JM; Suh GI; Shin HY; Kim SM; Sunwoo IN; Suh BC; Choi YC
    J Korean Med Sci; 2012 Apr; 27(4):423-9. PubMed ID: 22468107
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotypic and genotypic analysis of limb-Girdle muscular dystrophy type 2B.
    Aldosari KH; Al-Ghamdi S; Alkhathlan KM; Alkhalidi HM
    Neurosciences (Riyadh); 2020 Jul; 25(3):214-217. PubMed ID: 32683403
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a novel heterozygous DYSF variant in a large family with a dominantly-inherited dysferlinopathy.
    Folland C; Johnsen R; Botero Gomez A; Trajanoski D; Davis MR; Moore U; Straub V; Barresi R; Guglieri M; Hayhurst H; Schaefer AM; Laing NG; Lamont PJ; Ravenscroft G
    Neuropathol Appl Neurobiol; 2022 Dec; 48(7):e12846. PubMed ID: 35962550
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dysferlin deficiency treated like refractory polymyositis.
    Vinit J; Samson M; Gaultier JB; Laquerriere A; Ollagnon E; Petiot P; Marie I; Levesque H; Rousset H
    Clin Rheumatol; 2010 Jan; 29(1):103-6. PubMed ID: 19730931
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Progressive muscular weakness of lower limbs revealing a limb girdle muscular dystrophy].
    Saintmard G; Brands G; Debray FG; Lognard M
    Rev Med Liege; 2017 Jul; 72(7-8):373-376. PubMed ID: 28795552
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Compound heterozygous DYSF variants causing limb-girdle muscular dystrophy type 2B in a Chinese family.
    Li L; Jing Z; Cheng L; Liu W; Wang H; Xu Y; Zheng X; Yu X; Liu S
    J Gene Med; 2020 Nov; 22(11):e3272. PubMed ID: 32889728
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].
    Ren SC; Yan CZ; Li MX; Liu SP; Wu JL; Zhao YY; Li W; Li DN
    Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(21):1486-90. PubMed ID: 17785089
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Dysferlinopathy masquerading as a refractory polymyositis].
    Loureiro Amigo J; Gallardo E; Gallano P; Grau-Junyent JM
    Med Clin (Barc); 2015 Nov; 145(9):414-5. PubMed ID: 25662721
    [No Abstract]   [Full Text] [Related]  

  • 15. Diagnosis by protein analysis of dysferlinopathy in two patients mistaken as polymyositis.
    Angelini C; Grisold W; Nigro V
    Acta Myol; 2011 Dec; 30(3):185-7. PubMed ID: 22616201
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Late-onset dysferlinopathy presented as "liver enzyme" abnormalities: a technical note.
    Li F; Yin G; Xie Q; Shi G
    J Clin Rheumatol; 2014 Aug; 20(5):275-7. PubMed ID: 25036559
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CD4+ cells, macrophages, MHC-I and C5b-9 involve the pathogenesis of dysferlinopathy.
    Yin X; Wang Q; Chen T; Niu J; Ban R; Liu J; Mao Y; Pu C
    Int J Clin Exp Pathol; 2015; 8(3):3069-75. PubMed ID: 26045819
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Novel Homozygous Variant in DYSF Gene Is Associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B.
    Spadafora P; Qualtieri A; Cavalcanti F; Di Palma G; Gallo O; De Benedittis S; Cerantonio A; Citrigno L
    Int J Mol Sci; 2022 Aug; 23(16):. PubMed ID: 36012197
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Miyoshi Muscular Dystrophy Type 1 with Mutated
    Park J; Moon YJ; Kim DS
    Genes (Basel); 2023 Jan; 14(1):. PubMed ID: 36672942
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.