-
1
-
-
0026906885
-
Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
-
Van den Ouweland JM, Lemkes HH, Ruitenbeek W, et al.. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet, 1992, 1, 368-71.
-
(1992)
Nat Genet
, vol.1
, pp. 368-371
-
-
Van Den Ouweland, J.M.1
Lemkes, H.H.2
Ruitenbeek, W.3
-
2
-
-
0025666322
-
Mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Goto Y, Nonaka I, Horai S. Mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature, 1990, 348, 651-3.
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
3
-
-
0035341093
-
Maternally inherited diabetes and deafness: A multicenter study
-
Guillausseau PJ, Massin P, Dubois-LaForgue D, et al.. Maternally inherited diabetes and deafness: a multicenter study. Ann Intern Med, 2001, 134, 721-8.
-
(2001)
Ann Intern Med
, vol.134
, pp. 721-728
-
-
Guillausseau, P.J.1
Massin, P.2
Dubois-LaForgue, D.3
-
4
-
-
0035955922
-
Prevalence of gastrointestinal symptoms associated with diabetes mellitus: A population-based survey of 15,000 adults
-
Bytzer P, Talley NJ, Leemon M, Young LJ, Jones MP, Horowitz M. Prevalence of gastrointestinal symptoms associated with diabetes mellitus: a population-based survey of 15,000 adults. Arch Intern Med, 2001, 161, 1989-96.
-
(2001)
Arch Intern Med
, vol.161
, pp. 1989-1996
-
-
Bytzer, P.1
Talley, N.J.2
Leemon, M.3
Young, L.J.4
Jones, M.P.5
Horowitz, M.6
-
5
-
-
0034626387
-
Gastrointestinal tract symptoms among persons with diabetes mellitus in the community
-
Maleki D, Locke GR 3rd, Camilleri M, et al.. Gastrointestinal tract symptoms among persons with diabetes mellitus in the community. Arch Intern Med, 2000, 160, 2808-16.
-
(2000)
Arch Intern Med
, vol.160
, pp. 2808-2816
-
-
Maleki, D.1
Locke III, G.R.2
Camilleri, M.3
-
6
-
-
0030832950
-
Phenotypic expression of diabetes secondary to a T 14709 C mutation of mitochondrial DNA. Comparison with the MIDD syndrome (A 3243 G mutation)
-
Vialettes B, Paquis-Fluckinger V, Pelissier JF. Phenotypic expression of diabetes secondary to a T 14709 C mutation of mitochondrial DNA. Comparison with the MIDD syndrome (A 3243 G mutation). Diabetes Care, 1997, 20, 1731-7.
-
(1997)
Diabetes Care
, vol.20
, pp. 1731-1737
-
-
Vialettes, B.1
Paquis-Fluckinger, V.2
Pelissier, J.F.3
-
7
-
-
1842507464
-
Mitochondrial dysfunction and the gastrointestinal system
-
C. Desnuelle, S. DiMauro, Eds Springer-Verlag, France
-
Bindoff L. Mitochondrial dysfunction and the gastrointestinal system. In Mitochondrial Disorders: from pathophysiology to acquired defects. C. Desnuelle, S. DiMauro, Eds Springer-Verlag, France, 2002, 275-85.
-
(2002)
Mitochondrial Disorders: From Pathophysiology to Acquired Defects
, pp. 275-285
-
-
Bindoff, L.1
-
8
-
-
0023619281
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration
-
Yamamoto M, Sato T, Anno M, Ujike H, Takemoto M. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration. J Neurol Neurosurg Psychiatry, 1987, 50, 1475-81.
-
(1987)
J Neurol Neurosurg Psychiatry
, vol.50
, pp. 1475-1481
-
-
Yamamoto, M.1
Sato, T.2
Anno, M.3
Ujike, H.4
Takemoto, M.5
-
9
-
-
0023768385
-
Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type
-
Peiffer J, Kustermann-Kuhn B, Morder W, et al.. Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type. Pathol Res Pract, 1988, 183, 706-16.
-
(1988)
Pathol Res Pract
, vol.183
, pp. 706-716
-
-
Peiffer, J.1
Kustermann-Kuhn, B.2
Morder, W.3
-
10
-
-
0027530656
-
Clinical and autopsy findings in two cases of MELAS presenting with stroke-like episodes but without clinical myopathy
-
Nicoll JA, Moss TH, Love S, Campbell MJ, Schutt WH. Clinical and autopsy findings in two cases of MELAS presenting with stroke-like episodes but without clinical myopathy. Clin Neuropathol, 1993, 1, 38-43.
-
(1993)
Clin Neuropathol
, vol.1
, pp. 38-43
-
-
Nicoll, J.A.1
Moss, T.H.2
Love, S.3
Campbell, M.J.4
Schutt, W.H.5
-
11
-
-
0031861971
-
Mitochondrial encephalomyopathy showing prominent microvacuolation and necrosis of intestinal smooth muscle cells: A case diagnosed by rectal biopsy
-
Kuroiwa T, Kuwata T, Nakayama T, et al.. Mitochondrial encephalomyopathy showing prominent microvacuolation and necrosis of intestinal smooth muscle cells: a case diagnosed by rectal biopsy. Acta Neuropathol(Berl), 1998, 96, 86-90.
-
(1998)
Acta Neuropathol(Berl)
, vol.96
, pp. 86-90
-
-
Kuroiwa, T.1
Kuwata, T.2
Nakayama, T.3
-
12
-
-
0031648596
-
Familial occurrence of intestinal obstruction in children with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)
-
Shimotake T, Furukawa T, Inoue K, Iwai N, Takeuchi Y. Familial occurrence of intestinal obstruction in children with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS). J Pediatr Surg, 1998, 33, 1837-9.
-
(1998)
J Pediatr Surg
, vol.33
, pp. 1837-1839
-
-
Shimotake, T.1
Furukawa, T.2
Inoue, K.3
Iwai, N.4
Takeuchi, Y.5
-
13
-
-
0031823432
-
Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
-
Hiel JAP, Verrips A, Keyser A, et al.. Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes. Netherlands J Medicine, 1998, 53, 27-31.
-
(1998)
Netherlands J Medicine
, vol.53
, pp. 27-31
-
-
Hiel, J.A.P.1
Verrips, A.2
Keyser, A.3
-
14
-
-
0035116323
-
De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring
-
Ko CH, Lam CW, Tse PW, Kong CK, Chan AK, Wong LJ. De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring. J Paediatr Child Health, 2001, 37, 87-90.
-
(2001)
J Paediatr Child Health
, vol.37
, pp. 87-90
-
-
Ko, C.H.1
Lam, C.W.2
Tse, P.W.3
Kong, C.K.4
Chan, A.K.5
Wong, L.J.6
-
15
-
-
0037155616
-
Intestinal pseudoobstructions and gastric necrosis in mitochondrial myopathy
-
Muehlenberg K, Fiedler A, Schaumann I, Muller-Felber W, Wiedmann KH. Intestinal pseudoobstructions and gastric necrosis in mitochondrial myopathy. Dtsch Med Wochenschr, 2002, 127, 611-5.
-
(2002)
Dtsch Med Wochenschr
, vol.127
, pp. 611-615
-
-
Muehlenberg, K.1
Fiedler, A.2
Schaumann, I.3
Muller-Felber, W.4
Wiedmann, K.H.5
-
16
-
-
0029840031
-
Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in stroke-like episodes
-
Gilchrist JM, Sikirica M, Stopa E, Shanske S. Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in stroke-like episodes. Stroke, 1996, 27, 1420-3.
-
(1996)
Stroke
, vol.27
, pp. 1420-1423
-
-
Gilchrist, J.M.1
Sikirica, M.2
Stopa, E.3
Shanske, S.4
-
17
-
-
0033774734
-
Mitochondrial encephalomyopathy with lactic acidosis and stroke like episodes (MELAS) with prominent degeneration of the intestinal wall and cactus-like cerebellar pathology
-
Mori O, Yamazaki M, Ohaki Y, et al.. Mitochondrial encephalomyopathy with lactic acidosis and stroke like episodes (MELAS) with prominent degeneration of the intestinal wall and cactus-like cerebellar pathology. Acta Neuropathol (Berl), 2000, 100, 712-7.
-
(2000)
Acta Neuropathol (Berl)
, vol.100
, pp. 712-717
-
-
Mori, O.1
Yamazaki, M.2
Ohaki, Y.3
-
18
-
-
0028966152
-
Mitochondrial mutation in diabetic patient with gastrointestinal symptoms
-
letter
-
Kishimoto M, Hashiramoto M, Kanda F, Tanaka M, Kasuga M. Mitochondrial mutation in diabetic patient with gastrointestinal symptoms. Lancet, 1995, 345, 452 (letter).
-
(1995)
Lancet
, vol.345
, pp. 452
-
-
Kishimoto, M.1
Hashiramoto, M.2
Kanda, F.3
Tanaka, M.4
Kasuga, M.5
-
19
-
-
0019969786
-
Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis
-
Kobayashi Y, Miyabayashi S, Takada G, Narisawa K, Tada K, Yamamoto TY. Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis. Eur J Pediatr, 1982, 139, 25-30.
-
(1982)
Eur J Pediatr
, vol.139
, pp. 25-30
-
-
Kobayashi, Y.1
Miyabayashi, S.2
Takada, G.3
Narisawa, K.4
Tada, K.5
Yamamoto, T.Y.6
-
20
-
-
0029960177
-
Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging
-
't Hart LM, Jansen JJ, Lemkes HPJ, de Knijff P, Maasen JA. Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging. Human Mutation, 1996, 7, 193-7.
-
(1996)
Human Mutation
, vol.7
, pp. 193-197
-
-
'T Hart, L.M.1
Jansen, J.J.2
Lemkes, H.P.J.3
De Knijff, P.4
Maasen, J.A.5
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