AAAAAA

   
Results: 1-25 | 26-32 |
Results: 26-32/32
DETECTION OF PLATELET MITOCHONDRIAL-DNA DELETIONS IN KEARNS-SAYRE-SYNDROME (VOL 32, PG 2668, 1994)
Authors: OTA Y TANAKA M SATO W
Citation: Y. Ota et al., DETECTION OF PLATELET MITOCHONDRIAL-DNA DELETIONS IN KEARNS-SAYRE-SYNDROME (VOL 32, PG 2668, 1994), Investigative ophthalmology & visual science, 36(1), 1995, pp. 3-3
IDENTIFICATION AND EXPRESSION OF A MISSENSE MUTATION (Y446C) IN THE ACID SPHINGOMYELINASE GENE FROM A JAPANESE PATIENT WITH TYPE-A NIEMANN-PICK DISEASE
Authors: TAKAHASHI T SUCHI M SATO W TEN SB SAKURAGAWA N DESNICK RJ SCHUCHMAN EH TAKADA G
Citation: T. Takahashi et al., IDENTIFICATION AND EXPRESSION OF A MISSENSE MUTATION (Y446C) IN THE ACID SPHINGOMYELINASE GENE FROM A JAPANESE PATIENT WITH TYPE-A NIEMANN-PICK DISEASE, Tohoku Journal of Experimental Medicine, 177(2), 1995, pp. 117-123
A MITOCHONDRIAL TRNA(LEU(UUR)) MUTATION AT 3,256 ASSOCIATED WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES (MELAS)
Authors: SATO W HAYASAKA K SHOJI Y TAKAHASHI T TAKADA G SAITO M FUKAWA O WACHI E
Citation: W. Sato et al., A MITOCHONDRIAL TRNA(LEU(UUR)) MUTATION AT 3,256 ASSOCIATED WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES (MELAS), Biochemistry and molecular biology international, 33(6), 1994, pp. 1055-1061
A T-TO-C SUBSTITUTION AT NUCLEOTIDE-12311 IN TRNA(LEU(CUN)) GENE MAY BE A MTDNA POLYMORPHISM
Authors: SATO W HAYASAKA K
Citation: W. Sato et K. Hayasaka, A T-TO-C SUBSTITUTION AT NUCLEOTIDE-12311 IN TRNA(LEU(CUN)) GENE MAY BE A MTDNA POLYMORPHISM, Journal of the neurological sciences, 127(2), 1994, pp. 236-236
CARDIOMYOPATHY AND ANGIOPATHY IN PATIENTS WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES
Authors: SATO W TANAKA M SUGIYAMA S NEMOTO T HARADA K MIURA Y KOBAYASHI Y GOTO A TAKADA G OZAWA T
Citation: W. Sato et al., CARDIOMYOPATHY AND ANGIOPATHY IN PATIENTS WITH MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES, The American heart journal, 128(4), 1994, pp. 733-741
CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1B IS ASSOCIATED WITH MUTATIONS OF THE MYELIN-P(0) GENE
Authors: HAYASAKA K HIMORO M SATO W TAKADA G UYEMURA K SHIMIZU N BIRD TD CONNEALLY PM CHANCE PF
Citation: K. Hayasaka et al., CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1B IS ASSOCIATED WITH MUTATIONS OF THE MYELIN-P(0) GENE, Nature genetics, 5(1), 1993, pp. 31-34
MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES (MELAS) DECREASE IN DIASTOLIC LEFT-VENTRICULAR FUNCTION ASSESSED BY ECHOCARDIOGRAPHY
Authors: SUZUKI Y HARADA K MIURA Y SATO W HAYASAKA K KAWAMURA K TAKADA G
Citation: Y. Suzuki et al., MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKE-LIKE EPISODES (MELAS) DECREASE IN DIASTOLIC LEFT-VENTRICULAR FUNCTION ASSESSED BY ECHOCARDIOGRAPHY, Pediatric cardiology, 14(3), 1993, pp. 162-166
Risultati: 1-25 | 26-32 |