-
1
-
-
84902222203
-
Disease caused by genetic defects of mitochondria
-
th ed, Volume 1, 404.
-
th Ed.
, vol.1
, pp. 404
-
-
Anthony, S.1
-
2
-
-
0034096975
-
Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
-
Nishino I, Spinazzola A, Papadimitriou A, et al. Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. Ann Neurol 2000; 47: 792-800.
-
(2000)
Ann Neurol
, vol.47
, pp. 792-800
-
-
Nishino, I.1
Spinazzola, A.2
Papadimitriou, A.3
-
3
-
-
0030843425
-
A novel mitochondrial mutation G8313A associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathy
-
Verma A, Piccoli DA, Bonilla E, et al. A novel mitochondrial mutation G8313A associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathy. Pediatr Res 1997; 42: 448-54.
-
(1997)
Pediatr Res
, vol.42
, pp. 448-454
-
-
Verma, A.1
Piccoli, D.A.2
Bonilla, E.3
-
5
-
-
0028301915
-
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical and genetic features of an autosomal recessive mitochondrial disorder
-
Hirano M, Silvestri G, Blake DM, et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical and genetic features of an autosomal recessive mitochondrial disorder. Neurology 1994; 44: 721-7.
-
(1994)
Neurology
, vol.44
, pp. 721-727
-
-
Hirano, M.1
Silvestri, G.2
Blake, D.M.3
-
6
-
-
0031681413
-
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
-
Papadimitriou A, Comi GP, Hadjigeorgiou GM, et al. Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome. Neurology 1988; 51: 1086-92.
-
(1988)
Neurology
, vol.51
, pp. 1086-1092
-
-
Papadimitriou, A.1
Comi, G.P.2
Hadjigeorgiou, G.M.3
-
7
-
-
0016884709
-
Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria
-
Okamura K, Santa T, Nagae K, et al. Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria. J Neurol Sci 1976; 27: 79-91.
-
(1976)
J Neurol Sci
, vol.27
, pp. 79-91
-
-
Okamura, K.1
Santa, T.2
Nagae, K.3
-
8
-
-
0020567546
-
Oculogastrointestinal muscular dystrophy
-
Jonasescu V. Oculogastrointestinal muscular dystrophy. Am J Med Gen 1983; 15: 103-12.
-
(1983)
Am J Med Gen
, vol.15
, pp. 103-112
-
-
Jonasescu, V.1
-
9
-
-
0033067275
-
Mitochondrial neurogastrointestinal encephalomyopathy: Manometric and diagnostic features
-
Mueller LA, Camilleri M, Emslie-Smith AM. Mitochondrial neurogastrointestinal encephalomyopathy: manometric and diagnostic features. Gastroenterology 1999; 116: 959-63.
-
(1999)
Gastroenterology
, vol.116
, pp. 959-963
-
-
Mueller, L.A.1
Camilleri, M.2
Emslie-Smith, A.M.3
-
10
-
-
0023927307
-
Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathy
-
Cervera R, Bruix J, Bayes A. Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathy. Gut 1988; 29: 544-7.
-
(1988)
Gut
, vol.29
, pp. 544-547
-
-
Cervera, R.1
Bruix, J.2
Bayes, A.3
-
12
-
-
0019211636
-
Chronic idiopathic intestinal pseudoobstruction. A surgical approach
-
Schuffler MD, Deitch EA. Chronic idiopathic intestinal pseudoobstruction. A surgical approach. Ann Surg 1980; 192: 752-61.
-
(1980)
Ann Surg
, vol.192
, pp. 752-761
-
-
Schuffler, M.D.1
Deitch, E.A.2
-
13
-
-
0020359732
-
Pseudoobstruction and other obstructive disorders
-
Snape WJ Jr. Pseudoobstruction and other obstructive disorders. Clin Gastroenterol 1982; 11: 593-608.
-
(1982)
Clin Gastroenterol
, vol.11
, pp. 593-608
-
-
Snape Jr., W.J.1
-
14
-
-
0015374413
-
Esophageal and colon changes in myotonia dystrophica
-
Goldberg HI, Sheft DJ. Esophageal and colon changes in myotonia dystrophica. Gastroenterology 1972; 63: 134-9.
-
(1972)
Gastroenterology
, vol.63
, pp. 134-139
-
-
Goldberg, H.I.1
Sheft, D.J.2
-
16
-
-
0014734519
-
Dermatomyositis and its manifestations in the gastrointestinal tract
-
Kletchner FS. Dermatomyositis and its manifestations in the gastrointestinal tract. Am J Gastroenterol 1970; 53: 141.
-
(1970)
Am J Gastroenterol
, vol.53
, pp. 141
-
-
Kletchner, F.S.1
-
17
-
-
0015309883
-
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers
-
Olson W, Engel WK, Walsh GO, et al. Oculocraniosomatic neuromuscular disease with "ragged-red" fibers. Arch Neurol 1972; 26: 193-211.
-
(1972)
Arch Neurol
, vol.26
, pp. 193-211
-
-
Olson, W.1
Engel, W.K.2
Walsh, G.O.3
|