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4. Primary skeletal muscle involvement in chorea-acanthocytosis. Saiki S; Sakai K; Murata KY; Saiki M; Nakanishi M; Kitagawa Y; Kaito M; Gondo Y; Kumamoto T; Matsui M; Hattori N; Hirose G Mov Disord; 2007 Apr; 22(6):848-52. PubMed ID: 17345646 [TBL] [Abstract][Full Text] [Related]
5. Clinical features and molecular bases of neuroacanthocytosis. Rampoldi L; Danek A; Monaco AP J Mol Med (Berl); 2002 Aug; 80(8):475-91. PubMed ID: 12185448 [TBL] [Abstract][Full Text] [Related]
6. [An adult case of congenital myopathy--coexistence of nemaline rods and core-like structures]. Eto K; Watanabe T; Ida M; Kojima S; Takagi A; Narui K Rinsho Shinkeigaku; 1994 Jan; 34(1):43-7. PubMed ID: 8156709 [TBL] [Abstract][Full Text] [Related]
7. Intranuclear nemaline rod myopathy. Kaimaktchiev V; Goebel H; Laing N; Narus M; Weeks D; Nixon R Muscle Nerve; 2006 Sep; 34(3):369-72. PubMed ID: 16477620 [TBL] [Abstract][Full Text] [Related]
8. Adolescent obsessive compulsive disorder heralding chorea-acanthocytosis. Walterfang M; Yucel M; Walker R; Evans A; Bader B; Ng A; Danek A; Mocellin R; Velakoulis D Mov Disord; 2008 Feb; 23(3):422-5. PubMed ID: 18058950 [TBL] [Abstract][Full Text] [Related]
9. Nemaline myopathy: description of an adult onset case. Ginanneschi F; Mondelli M; Malandrini A; Gambelli S; Dotti MT; Federico A J Submicrosc Cytol Pathol; 2002 Jan; 34(1):105-8. PubMed ID: 11989852 [TBL] [Abstract][Full Text] [Related]
10. [Adult-onset nemaline myopathy with distal muscle atrophy--case report]. Niwa F; Shiga K; Kimura M; Yamaguchi T; Kondo M; Nakagawa M Brain Nerve; 2009 Jun; 61(6):695-9. PubMed ID: 19526838 [TBL] [Abstract][Full Text] [Related]
11. Chorea-acanthocytosis: a mimicker of Huntington disease case report and review of the literature. Gold MM; Shifteh K; Bello JA; Lipton M; Kaufman DM; Brown AD Neurologist; 2006 Nov; 12(6):327-9. PubMed ID: 17122731 [TBL] [Abstract][Full Text] [Related]
12. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred. Hutchinson DO; Charlton A; Laing NG; Ilkovski B; North KN Neuromuscul Disord; 2006 Feb; 16(2):113-21. PubMed ID: 16427282 [TBL] [Abstract][Full Text] [Related]
13. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2). Tajsharghi H; Ohlsson M; Lindberg C; Oldfors A Arch Neurol; 2007 Sep; 64(9):1334-8. PubMed ID: 17846275 [TBL] [Abstract][Full Text] [Related]
14. Idiopathic adult-onset nemaline myopathy presenting with isolated respiratory failure. Whitaker J; Love S; Williams AP; Plummeridge M Muscle Nerve; 2009 Mar; 39(3):406-8. PubMed ID: 19208402 [TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci. Jeannet PY; Mittaz L; Dunand M; Lobrinus JA; Bonafe L; Kuntzer T Neuromuscul Disord; 2007 Jan; 17(1):6-12. PubMed ID: 17157023 [TBL] [Abstract][Full Text] [Related]
16. Chorea-amyotrophy with chronic hemolytic anemia: a variant of chorea-amyotrophy with acanthocytosis. Spencer SE; Walker FO; Moore SA Neurology; 1987 Apr; 37(4):645-9. PubMed ID: 3561776 [TBL] [Abstract][Full Text] [Related]
17. Increased membrane protein phosphorylation and anion transport activity in chorea-acanthocytosis. Olivieri O; De Franceschi L; Bordin L; Manfredi M; Miraglia del Giudice E; Perrotta S; De Vivo M; Guarini P; Corrocher R Haematologica; 1997; 82(6):648-53. PubMed ID: 9499662 [TBL] [Abstract][Full Text] [Related]
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20. [A case of chorea-acanthocytosis with dilated cardiomyopathy and myopathy]. Kageyama Y; Kodama Y; Tadano M; Yamamoto S; Ichikawa K Rinsho Shinkeigaku; 2000 Aug; 40(8):816-20. PubMed ID: 11218703 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]