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Results: 1-25 |
Results: 25
THE EXPANDING CLINICAL SPECTRUM OF THE NARP SYNDROME
Authors: MCGOWAN KA NAVIAUX RK BARSHOP BA NYHAN WL HAAS RH
Citation: Ka. Mcgowan et al., THE EXPANDING CLINICAL SPECTRUM OF THE NARP SYNDROME, Journal of investigative medicine, 46(1), 1998, pp. 86-86
ANALYSIS OF ORGANIC-ACIDS, AMINO-ACIDS, AND CARNITINE IN DOGS WITH LIPID STORAGE MYOPATHY
Authors: SHELTON GD NYHAN WL KASS PH BARSHOP BA HAAS RH
Citation: Gd. Shelton et al., ANALYSIS OF ORGANIC-ACIDS, AMINO-ACIDS, AND CARNITINE IN DOGS WITH LIPID STORAGE MYOPATHY, Muscle & nerve, 21(9), 1998, pp. 1202-1205
ABSORPTION, TOLERABILITY, AND EFFECTS ON MITOCHONDRIAL ACTIVITY OF ORAL COENZYME Q(10) IN PARKINSONIAN-PATIENTS
Authors: SHULTS CW BEAL MF FONTAINE D NAKANO K HAAS RH
Citation: Cw. Shults et al., ABSORPTION, TOLERABILITY, AND EFFECTS ON MITOCHONDRIAL ACTIVITY OF ORAL COENZYME Q(10) IN PARKINSONIAN-PATIENTS, Neurology, 50(3), 1998, pp. 793-795
COENZYME-Q(10) LEVELS CORRELATE WITH THE ACTIVITIES OF COMPLEXE-I ANDCOMPLEX-II III IN MITOCHONDRIA FROM PARKINSONIAN AND NONPARKINSONIAN SUBJECTS/
Authors: SHULTS CW HAAS RH PASSOV D BEAL MF
Citation: Cw. Shults et al., COENZYME-Q(10) LEVELS CORRELATE WITH THE ACTIVITIES OF COMPLEXE-I ANDCOMPLEX-II III IN MITOCHONDRIA FROM PARKINSONIAN AND NONPARKINSONIAN SUBJECTS/, Annals of neurology, 42(2), 1997, pp. 261-264
MITOCHONDRIAL-DNA POINT MUTATIONS IN PEDIATRIC MOVEMENT DISORDER AND PD PATIENTS
Authors: SOLBRIG MV HUA XY GAO HG HAAS RH SHULTS CW
Citation: Mv. Solbrig et al., MITOCHONDRIAL-DNA POINT MUTATIONS IN PEDIATRIC MOVEMENT DISORDER AND PD PATIENTS, Neurology, 48(3), 1997, pp. 3097-3097
ASSESSMENT OF COENZYME-Q10 ABSORPTION AND TOLERABILITY IN PARKINSONS-DISEASE
Authors: SHULTS CW BEAL F FONTAINE DA HAAS RH
Citation: Cw. Shults et al., ASSESSMENT OF COENZYME-Q10 ABSORPTION AND TOLERABILITY IN PARKINSONS-DISEASE, Neurology, 48(3), 1997, pp. 32001-32001
OSTEOPENIA IN RETT-SYNDROME
Authors: HAAS RH DIXON SD SARTORIS DJ HENNESSY MJ
Citation: Rh. Haas et al., OSTEOPENIA IN RETT-SYNDROME, The Journal of pediatrics, 131(5), 1997, pp. 771-774
DIABETES AND MITOCHONDRIAL ENCEPHALOMYOPATHY WITH LACTIC-ACIDOSIS ANDSTROKE-LIKE EPISODES (MELAS) - RADIOLABELED POLYMERASE CHAIN-REACTIONIS NECESSARY FOR ACCURATE DETECTION OF LOW PERCENTAGES OF MUTATION
Authors: SMITH ML HUA XY MARSDEN DL LIU D KENNAWAY NG NGO KY HAAS RH
Citation: Ml. Smith et al., DIABETES AND MITOCHONDRIAL ENCEPHALOMYOPATHY WITH LACTIC-ACIDOSIS ANDSTROKE-LIKE EPISODES (MELAS) - RADIOLABELED POLYMERASE CHAIN-REACTIONIS NECESSARY FOR ACCURATE DETECTION OF LOW PERCENTAGES OF MUTATION, The Journal of clinical endocrinology and metabolism, 82(9), 1997, pp. 2826-2831
NEUROLOGIC ABNORMALITIES IN INFANTILE-AUTISM
Authors: HAAS RH TOWNSEND J COURCHESNE E LINCOLN AJ SCHREIBMAN L YEUNGCOURCHESNE R
Citation: Rh. Haas et al., NEUROLOGIC ABNORMALITIES IN INFANTILE-AUTISM, Journal of child neurology, 11(2), 1996, pp. 84-92
REVERSE TRANSCRIPTION AND THE BIPOTENTIAL REPLICATION OF MITOCHONDRIAL-DNA
Authors: NAVIAUX RK BARSHOP BA NYHAN WL HAAS RH
Citation: Rk. Naviaux et al., REVERSE TRANSCRIPTION AND THE BIPOTENTIAL REPLICATION OF MITOCHONDRIAL-DNA, Annals of neurology, 40(2), 1996, pp. 29-29
DNA-POLYMERASE-GAMMA DEFICIENCY IN MITOCHONDRIAL DISEASE
Authors: NAVIAUX RK NASIRIAN F LONGENECKER AM SHELTON D BARSHOP BA NYHAN WL HAAS RH
Citation: Rk. Naviaux et al., DNA-POLYMERASE-GAMMA DEFICIENCY IN MITOCHONDRIAL DISEASE, Annals of neurology, 40(2), 1996, pp. 39-39
ACUTE BASAL GANGLIA INFARCTION IN PROPIONIC ACIDEMIA
Authors: HAAS RH MARSDEN DL CAPISTRANOESTRADA S HAMILTON R GRAFE MR WONG W NYHAN WL
Citation: Rh. Haas et al., ACUTE BASAL GANGLIA INFARCTION IN PROPIONIC ACIDEMIA, Journal of child neurology, 10(1), 1995, pp. 18-22
NEUROPATHOLOGY OF PROPIONIC ACIDEMIA - A REPORT OF 2 PATIENTS WITH BASAL GANGLIA LESIONS
Authors: HAMILTON RL HAAS RH NYHAN WL POWELL HC GRAFE MR
Citation: Rl. Hamilton et al., NEUROPATHOLOGY OF PROPIONIC ACIDEMIA - A REPORT OF 2 PATIENTS WITH BASAL GANGLIA LESIONS, Journal of child neurology, 10(1), 1995, pp. 25-30
LEBERS HEREDITARY OPTIC NEUROPATHY PLUS DYSTONIA IS CAUSED BY A MITOCHONDRIAL-DNA POINT MUTATION
Authors: SHOFFNER JM BROWN MD STUGARD C JUN AS POLLOCK S HAAS RH KAUFMAN A KOONTZ D KIM Y GRAHAM JR SMITH E DIXON J WALLACE DC
Citation: Jm. Shoffner et al., LEBERS HEREDITARY OPTIC NEUROPATHY PLUS DYSTONIA IS CAUSED BY A MITOCHONDRIAL-DNA POINT MUTATION, Annals of neurology, 38(2), 1995, pp. 163-169
LOW PLATELET MITOCHONDRIAL COMPLEX-I AND COMPLEX-II III ACTIVITY IN EARLY UNTREATED PARKINSONS-DISEASE/
Authors: HAAS RH NASIRIAN F NAKANO K WARD D PAY M HILL R SHULTS CW
Citation: Rh. Haas et al., LOW PLATELET MITOCHONDRIAL COMPLEX-I AND COMPLEX-II III ACTIVITY IN EARLY UNTREATED PARKINSONS-DISEASE/, Annals of neurology, 37(6), 1995, pp. 714-722
OXIDATIVE-METABOLISM IN RETT-SYNDROME .1. CLINICAL-STUDIES
Authors: HAAS RH LIGHT M RICE M BARSHOP BA
Citation: Rh. Haas et al., OXIDATIVE-METABOLISM IN RETT-SYNDROME .1. CLINICAL-STUDIES, Neuropediatrics, 26(2), 1995, pp. 90-94
OXIDATIVE-METABOLISM IN RETT-SYNDROME .2. BIOCHEMICAL AND MOLECULAR STUDIES
Authors: HAAS RH NASIRIAN F HUA X NAKANO K HENNESSY M
Citation: Rh. Haas et al., OXIDATIVE-METABOLISM IN RETT-SYNDROME .2. BIOCHEMICAL AND MOLECULAR STUDIES, Neuropediatrics, 26(2), 1995, pp. 95-99
CARBIDOPA-LEVODOPA AND SELEGILINE DO NOT AFFECT PLATELET MITOCHONDRIAL-FUNCTION IN EARLY PARKINSONISM
Authors: SHULTS CW NASIRIAN F WARD DM NAKANO K PAY M HILL LR HAAS RH
Citation: Cw. Shults et al., CARBIDOPA-LEVODOPA AND SELEGILINE DO NOT AFFECT PLATELET MITOCHONDRIAL-FUNCTION IN EARLY PARKINSONISM, Neurology, 45(2), 1995, pp. 344-348
NEUROPHARMACOLOGY OF PROGRESSIVE MYOCLONUS EPILEPSY - RESPONSE TO 5-HYDROXY-L-TRYPTOPHAN
Authors: PRANZATELLI MR TATE E HUANG Y HAAS RH BODENSTEINER J ASHWAL S FRANZ D
Citation: Mr. Pranzatelli et al., NEUROPHARMACOLOGY OF PROGRESSIVE MYOCLONUS EPILEPSY - RESPONSE TO 5-HYDROXY-L-TRYPTOPHAN, Epilepsia, 36(8), 1995, pp. 783-791
IMPAIRMENT IN SHIFTING ATTENTION IN AUTISTIC AND CEREBELLAR PATIENTS
Authors: COURCHESNE E TOWNSEND J AKSHOOMOFF NA SAITOH O YEUNGCOURCHESNE R LINCOLN AJ JAMES HE HAAS RH SCHREIBMAN L LAU L
Citation: E. Courchesne et al., IMPAIRMENT IN SHIFTING ATTENTION IN AUTISTIC AND CEREBELLAR PATIENTS, Behavioral neuroscience, 108(5), 1994, pp. 848-865
ABNORMALITY OF CEREBELLAR VERMIAN LOBULES VI AND VII IN PATIENTS WITHINFANTILE-AUTISM - IDENTIFICATION OF HYPOPLASTIC AND HYPERPLASTIC SUBGROUPS WITH MR-IMAGING
Authors: COURCHESNE E SAITOH O YEUNGCOURCHESNE R PRESS GA LINCOLN AJ HAAS RH SCHREIBMAN L
Citation: E. Courchesne et al., ABNORMALITY OF CEREBELLAR VERMIAN LOBULES VI AND VII IN PATIENTS WITHINFANTILE-AUTISM - IDENTIFICATION OF HYPOPLASTIC AND HYPERPLASTIC SUBGROUPS WITH MR-IMAGING, American journal of roentgenology, 162(1), 1994, pp. 123-130
CEREBELLAR HYPOPLASIA AND HYPERPLASIA IN INFANTILE-AUTISM
Authors: COURCHESNE E SAITOH O TOWNSEND JP YEUNGCOURCHESNE R PRESS GA LINCOLN AJ HAAS RH SCHREIBMAN L
Citation: E. Courchesne et al., CEREBELLAR HYPOPLASIA AND HYPERPLASIA IN INFANTILE-AUTISM, Lancet, 343(8888), 1994, pp. 63-64
CARBIDOPA LEVODOPA AND SELEGILINE DO NOT AFFECT PLATELET MITOCHONDRIAL-FUNCTION IN EARLY PARKINSONISM/
Authors: SHULTS CW NASIRIAN F WARD D NAKANO K PAY M HILL LR HAAS RH
Citation: Cw. Shults et al., CARBIDOPA LEVODOPA AND SELEGILINE DO NOT AFFECT PLATELET MITOCHONDRIAL-FUNCTION IN EARLY PARKINSONISM/, Neurology, 44(4), 1994, pp. 10000154-10000154
LOW PLATELET MITOCHONDRIAL COMPLEX-I ACTIVITY IN UNTREATED EARLY PARKINSON DISEASE
Authors: HAAS RH NASIRIAN F WARD D NAKANO K PAY M HILL LR SHULTS CW
Citation: Rh. Haas et al., LOW PLATELET MITOCHONDRIAL COMPLEX-I ACTIVITY IN UNTREATED EARLY PARKINSON DISEASE, Neurology, 44(4), 1994, pp. 10000178-10000178
THE NEUROPATHOLOGY OF PROPIONIC ACIDEMIA - A REPORT OF 2 ADDITIONAL CASES
Authors: HAMILTON RL HAAS RH NYHAN WL POWELL HC GRAFE MR
Citation: Rl. Hamilton et al., THE NEUROPATHOLOGY OF PROPIONIC ACIDEMIA - A REPORT OF 2 ADDITIONAL CASES, Journal of neuropathology and experimental neurology, 52(3), 1993, pp. 299-299
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