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7. ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases. Magri F; Colombo I; Del Bo R; Previtali S; Brusa R; Ciscato P; Scarlato M; Ronchi D; D'Angelo MG; Corti S; Moggio M; Bresolin N; Comi GP BMC Neurol; 2015 Sep; 15():172. PubMed ID: 26404900 [TBL] [Abstract][Full Text] [Related]
8. Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome. Luo S; Cai S; Maxwell S; Yue D; Zhu W; Qiao K; Zhu Z; Zhou L; Xi J; Lu J; Beeson D; Zhao C Neuromuscul Disord; 2017 Jun; 27(6):557-564. PubMed ID: 28433477 [TBL] [Abstract][Full Text] [Related]
9. Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study. Astrea G; Romano A; Angelini C; Antozzi CG; Barresi R; Battini R; Battisti C; Bertini E; Bruno C; Cassandrini D; Fanin M; Fattori F; Fiorillo C; Guerrini R; Maggi L; Mercuri E; Morani F; Mora M; Moro F; Pezzini I; Picillo E; Pinelli M; Politano L; Rubegni A; Sanseverino W; Savarese M; Striano P; Torella A; Trevisan CP; Trovato R; Zaraieva I; Muntoni F; Nigro V; D'Amico A; Santorelli FM; Orphanet J Rare Dis; 2018 Sep; 13(1):170. PubMed ID: 30257713 [TBL] [Abstract][Full Text] [Related]
10. Mutations in GMPPB Presenting with Pseudometabolic Myopathy. Panicucci C; Fiorillo C; Moro F; Astrea G; Brisca G; Trucco F; Pedemonte M; Lanteri P; Sciarretta L; Minetti C; Santorelli FM; Bruno C JIMD Rep; 2018; 38():23-31. PubMed ID: 28456886 [TBL] [Abstract][Full Text] [Related]
11. Limb-girdle muscular dystrophy due to GMPPB mutations: A case report and comprehensive literature review. Sun L; Shen D; Xiong T; Zhou Z; Lu X; Cui F Bosn J Basic Med Sci; 2020 May; 20(2):275-280. PubMed ID: 30684953 [TBL] [Abstract][Full Text] [Related]
12. Mobility shift of beta-dystroglycan as a marker of Sarkozy A; Torelli S; Mein R; Henderson M; Phadke R; Feng L; Sewry C; Ala P; Yau M; Bertoli M; Willis T; Hammans S; Manzur A; Sframeli M; Norwood F; Rakowicz W; Radunovic A; Vaidya SS; Parton M; Walker M; Marino S; Offiah C; Farrugia ME; Mamutse G; Marini-Bettolo C; Wraige E; Beeson D; Lochmüller H; Straub V; Bushby K; Barresi R; Muntoni F J Neurol Neurosurg Psychiatry; 2018 Jul; 89(7):762-768. PubMed ID: 29437916 [TBL] [Abstract][Full Text] [Related]
14. Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations. Raphael AR; Couthouis J; Sakamuri S; Siskind C; Vogel H; Day JW; Gitler AD Brain Res; 2014 Aug; 1575():66-71. PubMed ID: 24780531 [TBL] [Abstract][Full Text] [Related]
15. Limb girdle muscular dystrophy due to mutations in Østergaard ST; Johnson K; Stojkovic T; Krag T; De Ridder W; De Jonghe P; Baets J; Claeys KG; Fernández-Torrón R; Phillips L; Topf A; Colomer J; Nafissi S; Jamal-Omidi S; Bouchet-Seraphin C; Leturcq F; MacArthur DG; Lek M; Xu L; Nelson I; Straub V; Vissing J J Neurol Neurosurg Psychiatry; 2018 May; 89(5):506-512. PubMed ID: 29175898 [TBL] [Abstract][Full Text] [Related]
16. Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy. Li M; Dickson DW; Spiro AJ Arch Neurol; 1997 Dec; 54(12):1457-61. PubMed ID: 9400354 [TBL] [Abstract][Full Text] [Related]
17. Limb-girdle muscular dystrophy type 2I is not rare in Taiwan. Liang WC; Hayashi YK; Ogawa M; Wang CH; Huang WT; Nishino I; Jong YJ Neuromuscul Disord; 2013 Aug; 23(8):675-81. PubMed ID: 23800702 [TBL] [Abstract][Full Text] [Related]
18. A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients. Humphrey EL; Lacey E; Le LT; Feng L; Sciandra F; Morris CR; Hewitt JE; Holt I; Brancaccio A; Barresi R; Sewry CA; Brown SC; Morris GE Neuromuscul Disord; 2015 Jan; 25(1):32-42. PubMed ID: 25387694 [TBL] [Abstract][Full Text] [Related]
19. Expanding the phenotype of GMPPB mutations. Cabrera-Serrano M; Ghaoui R; Ravenscroft G; Johnsen RD; Davis MR; Corbett A; Reddel S; Sue CM; Liang C; Waddell LB; Kaur S; Lek M; North KN; MacArthur DG; Lamont PJ; Clarke NF; Laing NG Brain; 2015 Apr; 138(Pt 4):836-44. PubMed ID: 25681410 [TBL] [Abstract][Full Text] [Related]
20. Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders. Geis T; Rödl T; Topaloğlu H; Balci-Hayta B; Hinreiner S; Müller-Felber W; Schoser B; Mehraein Y; Hübner A; Zirn B; Hoopmann M; Reutter H; Mowat D; Schuierer G; Schara U; Hehr U; Kölbel H Orphanet J Rare Dis; 2019 Jul; 14(1):179. PubMed ID: 31311558 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]