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.
28. [Congenital myopathies]. Cabello A; Ricoy-Campo JR Rev Neurol; 2003 Oct 16-31; 37(8):779-86. PubMed ID: 14593641 [TBL] [Abstract][Full Text] [Related]
29. The structure and regulation of myotubularin phosphatases. Begley MJ; Dixon JE Curr Opin Struct Biol; 2005 Dec; 15(6):614-20. PubMed ID: 16289848 [TBL] [Abstract][Full Text] [Related]
30. Congenital myotubular myopathy with a novel MTM1 gene mutation in a premature infant presenting with ventilator dependency and intrahepatic cholestasis. Lee IC; Su PH; Chen JY; Hu JM; Lu JJ; Ng YY J Child Neurol; 2012 Jan; 27(1):99-104. PubMed ID: 21881007 [TBL] [Abstract][Full Text] [Related]
31. Characterization of mutations in fifty North American patients with X-linked myotubular myopathy. Herman GE; Kopacz K; Zhao W; Mills PL; Metzenberg A; Das S Hum Mutat; 2002 Feb; 19(2):114-21. PubMed ID: 11793470 [TBL] [Abstract][Full Text] [Related]
32. Genetic testing for myotubular myopathy despite muscle biopsy without centrally located nuclei. Foye PM Dev Med Child Neurol; 2006 Dec; 48(12):1011. PubMed ID: 17109798 [No Abstract] [Full Text] [Related]
33. X-linked myotubular myopathy and chylothorax. Smets K Neuromuscul Disord; 2008 Feb; 18(2):183-4. PubMed ID: 18077167 [TBL] [Abstract][Full Text] [Related]
34. Fatal hepatic hemorrhage by peliosis hepatis in X-linked myotubular myopathy: a case report. Motoki T; Fukuda M; Nakano T; Matsukage S; Fukui A; Akiyoshi S; Hayashi YK; Ishii E; Nishino I Neuromuscul Disord; 2013 Nov; 23(11):917-21. PubMed ID: 24011703 [TBL] [Abstract][Full Text] [Related]
35. X-linked myotubular myopathy with a novel MTM1 mutation in a Taiwanese child. Chang CY; Lin SP; Lin HY; Chuang CK; Ho CS; Su YN J Formos Med Assoc; 2008 Dec; 107(12):965-70. PubMed ID: 19129059 [TBL] [Abstract][Full Text] [Related]
36. [Unilateral presentation of X-linked myotubular myopathy (XLMTM) in two out of three female carriers in a family with no affected male]. Drouet A; Ollagnon-Roman E; Streichenberger N; Biancalana V; Cossée M; Guilloton L; Petiot P Rev Neurol (Paris); 2008 Feb; 164(2):169-76. PubMed ID: 18358876 [TBL] [Abstract][Full Text] [Related]
37. [X-linked myotubular myopathy. Muscle biopsy as a diagnostic tool in neonatal myopathy]. Dahl M; Schrøder HD; Hansen LK Ugeskr Laeger; 2005 Jun; 167(23):2532-3. PubMed ID: 16008013 [No Abstract] [Full Text] [Related]
38. A newborn with spinal muscular atrophy type 0 presenting with a clinicopathological picture suggestive of myotubular myopathy. Nadeau A; D'Anjou G; Debray G; Robitaille Y; Simard LR; Vanasse M J Child Neurol; 2007 Nov; 22(11):1301-4. PubMed ID: 18006961 [TBL] [Abstract][Full Text] [Related]
39. MRI in DNM2-related centronuclear myopathy: evidence for highly selective muscle involvement. Schessl J; Medne L; Hu Y; Zou Y; Brown MJ; Huse JT; Torigian DA; Jungbluth H; Goebel HH; Bönnemann CG Neuromuscul Disord; 2007 Jan; 17(1):28-32. PubMed ID: 17134899 [TBL] [Abstract][Full Text] [Related]
40. Mutation studies in X-linked myotubular myopathy in three Indian families. Bijarnia S; Puri RD; Jain M; Kler N; Roy S; Urtizberea JA; Biancalana V; Verma IC Indian J Pediatr; 2010 Apr; 77(4):431-3. PubMed ID: 20358311 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]