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 *

125 related articles for article (PubMed ID: 36317204)

  • 1. [Analysis of clinical features and genetic variants in three Chinese pedigrees affected with Limb girdle muscular dystrophy type 2I].
    Wang G; Xu L; Zhao D; Yan C; Lin P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Nov; 39(11):1205-1210. PubMed ID: 36317204
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients.
    Wang DN; Wang ZQ; Chen YQ; Xu GR; Lin MT; Wang N
    Int J Neurosci; 2018 Mar; 128(3):199-207. PubMed ID: 28931339
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Analysis of clinical characteristics and genetic variants in two children with Limb-girdle muscular dystrophy autosomal recessive 9 FKRP-related].
    Yu J; Xu M; Ding L; Huang Y; Guo H; He Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Oct; 40(10):1217-1221. PubMed ID: 37730220
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Asian patients with limb girdle muscular dystrophy 2I (LGMD2I).
    Hong D; Zhang W; Wang W; Wang Z; Yuan Y
    J Clin Neurosci; 2011 Apr; 18(4):494-9. PubMed ID: 21296577
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I.
    Boito CA; Melacini P; Vianello A; Prandini P; Gavassini BF; Bagattin A; Siciliano G; Angelini C; Pegoraro E
    Arch Neurol; 2005 Dec; 62(12):1894-9. PubMed ID: 16344347
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the
    Xie Z; Xiao J; Zheng Y; Wang Z; Yuan Y
    Biomed Res Int; 2018; 2018():3710814. PubMed ID: 30003095
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies.
    Fu X; Yang H; Wei C; Jiao H; Wang S; Yang Y; Han C; Wu X; Xiong H
    J Hum Genet; 2016 Dec; 61(12):1013-1020. PubMed ID: 27439679
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation.
    Belhassen I; Menassa R; Sakka S; Michel-Calemard L; Streichenberger N; Ayed DB; Bouattour N; Dammak M; Mhiri C
    Acta Myol; 2023; 42(4):106-112. PubMed ID: 38406381
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variants of CAPN3 cause limb-girdle muscular dystrophy type 2A in two Chinese families.
    Zheng J; Xu X; Zhang X; Wang X; Shu J; Cai C
    Exp Ther Med; 2021 Feb; 21(2):104. PubMed ID: 33335567
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analysis of DYSF gene mutations in two pedigrees affected with limb-girdle muscular dystrophy type 2B].
    Liu Z; Liao H; Zhang X; Zhang H; Liu H; Wang H; Liu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):498-501. PubMed ID: 30098242
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Muscle and heart function restoration in a limb girdle muscular dystrophy 2I (LGMD2I) mouse model by systemic FKRP gene delivery.
    Qiao C; Wang CH; Zhao C; Lu P; Awano H; Xiao B; Li J; Yuan Z; Dai Y; Martin CB; Li J; Lu Q; Xiao X
    Mol Ther; 2014 Nov; 22(11):1890-9. PubMed ID: 25048216
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy.
    Liang WC; Jong YJ; Wang CH; Wang CH; Tian X; Chen WZ; Kan TM; Minami N; Nishino I; Wong LC
    Orphanet J Rare Dis; 2020 Jun; 15(1):160. PubMed ID: 32576226
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies.
    Serafini PR; Feyder MJ; Hightower RM; Garcia-Perez D; Vieira NM; Lek A; Gibbs DE; Moukha-Chafiq O; Augelli-Szafran CE; Kawahara G; Widrick JJ; Kunkel LM; Alexander MS
    JCI Insight; 2018 Sep; 3(18):. PubMed ID: 30232282
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Limb girdle muscular dystrophy type 2I: No correlation between clinical severity, histopathology and glycosylated α-dystroglycan levels in patients homozygous for common FKRP mutation.
    Alhamidi M; Brox V; Stensland E; Liset M; Lindal S; Nilssen Ø
    Neuromuscul Disord; 2017 Jul; 27(7):619-626. PubMed ID: 28479227
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients.
    Awano H; Saito Y; Shimizu M; Sekiguchi K; Niijima S; Matsuo M; Maegaki Y; Izumi I; Kikuchi C; Ishibashi M; Okazaki T; Komaki H; Iijima K; Nishino I
    J Clin Neurosci; 2021 Oct; 92():215-221. PubMed ID: 34509255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy.
    Couthouis J; Raphael AR; Siskind C; Findlay AR; Buenrostro JD; Greenleaf WJ; Vogel H; Day JW; Flanigan KM; Gitler AD
    Neuromuscul Disord; 2014 May; 24(5):431-5. PubMed ID: 24594375
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patients.
    Bourteel H; Vermersch P; Cuisset JM; Maurage CA; Laforet P; Richard P; Stojkovic T
    J Neurol Neurosurg Psychiatry; 2009 Dec; 80(12):1405-8. PubMed ID: 19917824
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.