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Results: 1-25 |
Results: 25
CLN3 IN CANCER, DEVELOPMENT, AND SENESCENCE
Authors: GUO WX CHANG J PANE M BOUSTANY RM
Citation: Wx. Guo et al., CLN3 IN CANCER, DEVELOPMENT, AND SENESCENCE, Annals of neurology, 44(3), 1998, pp. 45-45
APOPTOSIS IN DEVELOPMENT AND DISEASE OF THE NERVOUS-SYSTEM .2. APOPTOSIS IN CHILDHOOD NEUROLOGIC DISEASE
Authors: GELBARD HA BOUSTANY RM SCHOR NF
Citation: Ha. Gelbard et al., APOPTOSIS IN DEVELOPMENT AND DISEASE OF THE NERVOUS-SYSTEM .2. APOPTOSIS IN CHILDHOOD NEUROLOGIC DISEASE, Pediatric neurology, 16(2), 1997, pp. 93-97
APOPTOSIS IN DEVELOPMENT AND DISEASE OF THE NERVOUS-SYSTEM .2. APOPTOSIS IN CHILDHOOD NEUROLOGIC DISEASE
Authors: GELBARD HA BOUSTANY RM SCHOR NF
Citation: Ha. Gelbard et al., APOPTOSIS IN DEVELOPMENT AND DISEASE OF THE NERVOUS-SYSTEM .2. APOPTOSIS IN CHILDHOOD NEUROLOGIC DISEASE, Pediatric neurology, 16(2), 1997, pp. 93-97
CLN3 DEFINES A NOVEL ANTIAPOPTOTIC PATHWAY OPERATIVE IN NEURODEGENERATION AND MEDIATED BY CERAMIDE
Authors: PURANAM KL QIAN WH NIKBAKHT K BOUSTANY RM
Citation: Kl. Puranam et al., CLN3 DEFINES A NOVEL ANTIAPOPTOTIC PATHWAY OPERATIVE IN NEURODEGENERATION AND MEDIATED BY CERAMIDE, Annals of neurology, 42(3), 1997, pp. 7-7
UP-REGULATION OF BCL-2 AND ELEVATION OF CERAMIDE IN BATTEN-DISEASE
Authors: PURANAM K QIAN WH NIKBAKHT K VENABLE M OBEID L HANNUN Y BOUSTANY RM
Citation: K. Puranam et al., UP-REGULATION OF BCL-2 AND ELEVATION OF CERAMIDE IN BATTEN-DISEASE, Neuropediatrics, 28(1), 1997, pp. 37-41
POLYUNSATURATED FATTY-ACIDS REVERSE THE LYSOSOMAL STORAGE AND ACCUMULATION OF SUBUNIT-9 OF MITOCHONDRIAL F1F0-ATP SYNTHASE IN CULTURED LYMPHOBLASTS FROM PATIENTS WITH BATTEN-DISEASE
Authors: BENNETT MJ BORIACK RL BOUSTANY RM
Citation: Mj. Bennett et al., POLYUNSATURATED FATTY-ACIDS REVERSE THE LYSOSOMAL STORAGE AND ACCUMULATION OF SUBUNIT-9 OF MITOCHONDRIAL F1F0-ATP SYNTHASE IN CULTURED LYMPHOBLASTS FROM PATIENTS WITH BATTEN-DISEASE, Journal of inherited metabolic disease, 20(3), 1997, pp. 457-460
CLN3 DEFINES A NOVEL ANTIAPOPTIC PATHWAY OPERATIVE IN NEURODEGENERATION AND MEDIATED VIA CERAMIDE
Authors: PURANAM KL QIAN WH NIKBAKHT K BOUSTANY RM
Citation: Kl. Puranam et al., CLN3 DEFINES A NOVEL ANTIAPOPTIC PATHWAY OPERATIVE IN NEURODEGENERATION AND MEDIATED VIA CERAMIDE, Journal of neurochemistry, 69, 1997, pp. 123-123
SPECTRUM OF MUTATIONS IN THE BATTEN-DISEASE GENE, CLN3
Authors: MUNROE PB MITCHISON HM ORAWE AM ANDERSON JW BOUSTANY RM LERNER TJ TASCHNER PEM DEVOS N BREUNING MH GARDINER RM MOLE SE
Citation: Pb. Munroe et al., SPECTRUM OF MUTATIONS IN THE BATTEN-DISEASE GENE, CLN3, American journal of human genetics, 61(2), 1997, pp. 310-316
REFRACTORY STATUS EPILEPTICUS ASSOCIATED WITH PROGRESSIVE MAGNETIC-RESONANCE-IMAGING SIGNAL CHANGE AND HIPPOCAMPAL NEURONAL LOSS
Authors: STAFSTROM CE TIEN RD MONTINE TJ BOUSTANY RM
Citation: Ce. Stafstrom et al., REFRACTORY STATUS EPILEPTICUS ASSOCIATED WITH PROGRESSIVE MAGNETIC-RESONANCE-IMAGING SIGNAL CHANGE AND HIPPOCAMPAL NEURONAL LOSS, Journal of epilepsy, 9(4), 1996, pp. 253-258
A COMMON MUTATION SITE IN THE BETA-GALACTOSIDASE GENE ORIGINATES IN PUERTO-RICO
Authors: CHIU NC QIAN WH SHANSKE AL BROOKS SS BOUSTANY RM
Citation: Nc. Chiu et al., A COMMON MUTATION SITE IN THE BETA-GALACTOSIDASE GENE ORIGINATES IN PUERTO-RICO, Pediatric neurology, 14(1), 1996, pp. 53-56
TORTICOLLIS ACQUIRED IN LATE INFANCY DUE TO A CEREBELLAR GANGLIOCYTOMA
Authors: CARESS JB NOHRIA V FUCHS H BOUSTANY RM
Citation: Jb. Caress et al., TORTICOLLIS ACQUIRED IN LATE INFANCY DUE TO A CEREBELLAR GANGLIOCYTOMA, International journal of pediatric otorhinolaryngology, 36(1), 1996, pp. 39-44
APOPTOSIS AS THE MECHANISM OF NEURODEGENERATION IN BATTENS DISEASE
Authors: LANE SC JOLLY RD SCHMECHEL DE ALROY J BOUSTANY RM
Citation: Sc. Lane et al., APOPTOSIS AS THE MECHANISM OF NEURODEGENERATION IN BATTENS DISEASE, Journal of neurochemistry, 67(2), 1996, pp. 677-683
ERYTHROMYCIN-INDUCED CARBAMAZEPINE TOXICITY - A CONTINUING PROBLEM
Authors: STAFSTROM CE NOHRIA V LOGANBILL H NAHOURAII R BOUSTANY RM DELONG GR
Citation: Ce. Stafstrom et al., ERYTHROMYCIN-INDUCED CARBAMAZEPINE TOXICITY - A CONTINUING PROBLEM, Archives of pediatrics & adolescent medicine, 149(1), 1995, pp. 99-101
APOPTOSIS IN INHERITED NEURODEGENERATIVE DISEASES
Authors: BOUSTANY RM LANE SC QIAN WH PURANAM K BURKE J
Citation: Rm. Boustany et al., APOPTOSIS IN INHERITED NEURODEGENERATIVE DISEASES, Annals of neurology, 38(3), 1995, pp. 525-525
ROLE OF SUBUNIT-9 OF MITOCHONDRIAL ATP SYNTHASE IN BATTEN-DISEASE
Authors: JOHNSON DW SPEIER S QIAN WH LANE S COOK A SUZUKI K DANIEL P BOUSTANY RM
Citation: Dw. Johnson et al., ROLE OF SUBUNIT-9 OF MITOCHONDRIAL ATP SYNTHASE IN BATTEN-DISEASE, American journal of medical genetics, 57(2), 1995, pp. 350-360
GENETIC-LOCUS HETEROGENEITY AND CLINICAL CLASSIFICATION OF AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA
Authors: HENTATI A PERICAKVANCE MA LENNON F HENTATI F LAING N HUNG WY BOUSTANY RM BOUHLEGA S BENHAMIDA M SIDDIQUE T
Citation: A. Hentati et al., GENETIC-LOCUS HETEROGENEITY AND CLINICAL CLASSIFICATION OF AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA, Neurology, 45(4), 1995, pp. 452-453
BATTEN-DISEASE .2. GENOMIC ALTERATIONS IN CLN3
Authors: TASCHNER PEM MITCHISON HM KREMMIDIOTIS G ORAWE A MUNROE PB DEVOS N BOUSTANY RM LENSINK I MEINCKE LJ ANDERSON JW DARIGO KL JARVELA IE BUCKLER AJ GUSELLA JF HAINES JL GARDINER RM SUTHERLAND GR DOGGETT NA CALLEN DF MOLE SE LERNER TJ BREUNING MH
Citation: Pem. Taschner et al., BATTEN-DISEASE .2. GENOMIC ALTERATIONS IN CLN3, American journal of human genetics, 57(4), 1995, pp. 1328-1328
LINKAGE OF PURE AUTOSOMAL RECESSIVE FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME-8 MARKERS AND EVIDENCE OF GENETIC-LOCUS HETEROGENEITY
Authors: HENTATI A PERICAKVANCE MA HUNG WY BELAL S LAING N BOUSTANY RM HENTATI F HAMIDA MB SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF PURE AUTOSOMAL RECESSIVE FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME-8 MARKERS AND EVIDENCE OF GENETIC-LOCUS HETEROGENEITY, Human molecular genetics, 3(8), 1994, pp. 1263-1267
LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIATO CHROMOSOME 2P MARKERS
Authors: HENTATI A PERICAKVANCE MA LENNON F WASSERMAN B HENTATI F JUNEJA T ANGRIST MH HUNG WY BOUSTANY RM BOHLEGA S IQBAL Z HUETHER CH BENHAMIDA M SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIATO CHROMOSOME 2P MARKERS, Human molecular genetics, 3(10), 1994, pp. 1867-1871
A SPLICE JUNCTION MUTATION IN A NEW MYOPATHIC VARIANT OF PHOSPHOGLYCERATE KINASE-DEFICIENCY (PGK NORTH-CAROLINA)
Authors: TSUJINO S TONIN P SHANSKE S NOHRIA V BOUSTANY RM LEWIS D CHEN YT DIMAURO S
Citation: S. Tsujino et al., A SPLICE JUNCTION MUTATION IN A NEW MYOPATHIC VARIANT OF PHOSPHOGLYCERATE KINASE-DEFICIENCY (PGK NORTH-CAROLINA), Annals of neurology, 35(3), 1994, pp. 349-353
LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIATO CHROMOSOME 2P MARKERS
Authors: HENTATI A PERICAKVANCE MA LENNON F WASSERMAN B HENTATI F JUNEJA T ANGRIST MH HUNG WY BOUSTANY RM BOHLEGA S IGBAL Z HUETHER CH HAMIDA MB SIDDIQUE T
Citation: A. Hentati et al., LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIATO CHROMOSOME 2P MARKERS, Cytogenetics and cell genetics, 67(4), 1994, pp. 244-244
FORE RECESSIVE FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE OF LINKAGE TO CHROMOSOME-8 AND GENETIC-LOCUS HETEROGENEITY
Authors: HENTATI A PERICAKVANCE MA HUNG WY BELAL S LAING N BOUSTANY RM HENTATI F BENHAMIDA M SIDDIQUE T
Citation: A. Hentati et al., FORE RECESSIVE FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE OF LINKAGE TO CHROMOSOME-8 AND GENETIC-LOCUS HETEROGENEITY, Neurology, 44(4), 1994, pp. 10000361-10000361
SEIZURES, DEPRESSION AND DEMENTIA IN TEENAGERS WITH BATTEN-DISEASE
Authors: BOUSTANY RM FILIPEK P
Citation: Rm. Boustany et P. Filipek, SEIZURES, DEPRESSION AND DEMENTIA IN TEENAGERS WITH BATTEN-DISEASE, Journal of inherited metabolic disease, 16(2), 1993, pp. 252-255
MUTATIONS IN ACID BETA-GALACTOSIDASE CAUSE GM(1)-GANGLIOSIDOSIS IN AMERICAN PATIENTS
Authors: BOUSTANY RM QIAN WH SUZUKI K
Citation: Rm. Boustany et al., MUTATIONS IN ACID BETA-GALACTOSIDASE CAUSE GM(1)-GANGLIOSIDOSIS IN AMERICAN PATIENTS, American journal of human genetics, 53(4), 1993, pp. 881-888
LINKAGE DISEQUILIBRIUM BETWEEN THE JUVENILE NCL GENE (CLN3) AND MARKER LOCI ON CHROMOSOME-16P12.1
Authors: LERNER T BOUSTANY RM SCHULTZ E DARIGO K SCHLUMPF K GUSELLA J HAINES J
Citation: T. Lerner et al., LINKAGE DISEQUILIBRIUM BETWEEN THE JUVENILE NCL GENE (CLN3) AND MARKER LOCI ON CHROMOSOME-16P12.1, American journal of human genetics, 53(3), 1993, pp. 1032-1032
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