BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 26304763)

  • 1. Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy.
    Ding J; Zhao D; Du R; Zhang Y; Yang H; Liu J; Yan C; Zhang F; Xiong H
    Brain Dev; 2016 Feb; 38(2):242-9. PubMed ID: 26304763
    [TBL] [Abstract][Full Text] [Related]  

  • 2. LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies.
    Løkken N; Born AP; Duno M; Vissing J
    Muscle Nerve; 2015 Oct; 52(4):547-53. PubMed ID: 25663498
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Limb girdle muscular dystrophy due to
    Magri F; Brusa R; Bello L; Peverelli L; Del Bo R; Govoni A; Cinnante C; Colombo I; Fortunato F; Tironi R; Corti S; Grimoldi N; Sciacco M; Bresolin N; Pegoraro E; Moggio M; Comi GP
    Acta Myol; 2020 Jun; 39(2):67-82. PubMed ID: 32904964
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients.
    Xiong H; Tan D; Wang S; Song S; Yang H; Gao K; Liu A; Jiao H; Mao B; Ding J; Chang X; Wang J; Wu Y; Yuan Y; Jiang Y; Zhang F; Wu H; Wu X
    Clin Genet; 2015 Mar; 87(3):233-43. PubMed ID: 24611677
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted next generation sequencing reveals a novel intragenic deletion of the LAMA2 gene in a patient with congenital muscular dystrophy.
    Yang Y; Mao B; Wang L; Mao L; Zhou A; Cao J; Hu J; Zhou Y; Pan Y; Wei X; Yang S; Mu F; Liu Z
    Mol Med Rep; 2015 May; 11(5):3687-93. PubMed ID: 25544356
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diagnosis and genetic testing analysis of limb-girdle muscular dystrophy type 2U caused by a compound heterozygous mutation in the
    Huang J; Miao WH; Guo XF; Ji W
    Yi Chuan; 2023 Jun; 45(6):536-542. PubMed ID: 37340967
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compound heterozygous
    Zhang C; Zheng X; Lu D; Xu L; Che F; Liu S
    Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33899113
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations.
    Gavassini BF; Carboni N; Nielsen JE; Danielsen ER; Thomsen C; Svenstrup K; Bello L; Maioli MA; Marrosu G; Ticca AF; Mura M; Marrosu MG; Soraru G; Angelini C; Vissing J; Pegoraro E
    Muscle Nerve; 2011 Nov; 44(5):703-9. PubMed ID: 21953594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.
    Naom I; D'Alessandro M; Sewry CA; Philpot J; Manzur AY; Dubowitz V; Muntoni F
    Neuromuscul Disord; 1998 Oct; 8(7):495-501. PubMed ID: 9829280
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy.
    Dai Y; Liang S; Dong X; Zhao Y; Ren H; Guan Y; Yin H; Li C; Chen L; Cui L; Banerjee S
    J Cell Mol Med; 2019 Feb; 23(2):811-818. PubMed ID: 30450679
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy.
    Kong X; Zhong X; Liu L; Cui S; Yang Y; Kong L
    BMC Med Genet; 2019 Aug; 20(1):139. PubMed ID: 31412794
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin-deficient congenital muscular dystrophy type 1A.
    Khorrami A; Goleij P; Karamad V; Taheri E; Shadman B; Emami P; Jahangirzadeh G; Hajazimian S; Isazadeh A; Baradaran B; Heidari M
    J Clin Lab Anal; 2021 Nov; 35(11):e23930. PubMed ID: 34528292
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in LAMA2 and CAPN3 genes associated with genetic and phenotypic heterogeneities within a single consanguineous family involving both congenital and progressive muscular dystrophies.
    Hadj Salem I; Kamoun F; Louhichi N; Rouis S; Mziou M; Fendri-Kriaa N; Makni-Ayadi F; Triki C; Fakhfakh F
    Biosci Rep; 2011 Apr; 31(2):125-35. PubMed ID: 20477750
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical, molecular pathological and genetic analyses of a Chinese family with congenital muscular dystrophy type 1A].
    Wang S; Xiong H; Luo J; Chang X; Yuan Y; Wu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb; 27(1):13-7. PubMed ID: 20140860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
    Tan D; Ge L; Fan Y; Chang X; Wang S; Wei C; Ding J; Liu A; Wang S; Li X; Gao K; Yang H; Que C; Huang Z; Li C; Zhu Y; Mao B; Jin B; Hua Y; Zhang X; Zhang B; Zhu W; Zhang C; Wang Y; Yuan Y; Jiang Y; Rutkowski A; Bönnemann CG; Wu X; Xiong H
    Orphanet J Rare Dis; 2021 Jul; 16(1):319. PubMed ID: 34281576
    [TBL] [Abstract][Full Text] [Related]  

  • 16. TRIM32 biallelic defects cause limb-girdle muscular dystrophy R8: identification of two novel mutations and investigation of genotype-phenotype correlation.
    Guan Y; Liang X; Li W; Lin W; Liang G; Xie H; Hou Y; Hu Y; Shang X
    Skelet Muscle; 2023 May; 13(1):10. PubMed ID: 37217920
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of
    Xu Y; Zhu L; Qian Y; Dong M
    Front Pediatr; 2023; 11():1191068. PubMed ID: 37404563
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case report: Adult-onset limb girdle muscular dystrophy in sibling pair due to novel homozygous
    Katz M; Waddell LB; Yuen M; Bryen SJ; Oates E; Garton FC; Robertson T; Henderson RD; Cooper ST; McCombe PA
    Front Neurol; 2023; 14():1055639. PubMed ID: 36779065
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Variant analysis for a pedigree affected with limb-girdle muscular dystrophy type 2D].
    Ding L; Tang S; Li H; Xu X; Luan Z; Zhang Q; Lyu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):136-139. PubMed ID: 30703231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.