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Results: 1-25 | 26-31
Results: 1-25/31
GENOTYPE-PHENOTYPE CORRESPONDENCE IN SANFILIPPO SYNDROME TYPE-B
Authors: ZHAO HG ARONOVICH EL WHITLEY CB
Citation: Hg. Zhao et al., GENOTYPE-PHENOTYPE CORRESPONDENCE IN SANFILIPPO SYNDROME TYPE-B, American journal of human genetics, 62(1), 1998, pp. 53-63
NAGLU MUTATIONS UNDERLYING SANFILIPPO SYNDROME TYPE-B
Authors: SCHMIDTCHEN A GREENBERG D ZHAO HG LI HH HUANG Y TIEU P ZHAO HZ CHENG SS ZHAO ZY WHITLEY CB DINATALE P NEUFELD EF
Citation: A. Schmidtchen et al., NAGLU MUTATIONS UNDERLYING SANFILIPPO SYNDROME TYPE-B, American journal of human genetics, 62(1), 1998, pp. 64-69
SYRINGOMYELIA IN MUCOPOLYSACCHARIDOSIS TYPE-VI (MAROTEAUX-LAMY-SYNDROME) - IMAGING FINDINGS FOLLOWING BONE-MARROW TRANSPLANTATION
Authors: HITE SH KRIVIT W HAINES SJ WHITLEY CB
Citation: Sh. Hite et al., SYRINGOMYELIA IN MUCOPOLYSACCHARIDOSIS TYPE-VI (MAROTEAUX-LAMY-SYNDROME) - IMAGING FINDINGS FOLLOWING BONE-MARROW TRANSPLANTATION, Pediatric radiology, 27(9), 1997, pp. 736-738
CLINICAL AND BIOCHEMICAL HETEROGENEITY IN FEMALES OF A LARGE PEDIGREEWITH ORNITHINE TRANSCARBAMYLASE DEFICIENCY DUE TO THE R141Q MUTATION (VOL 66, PG 311, 1996)
Authors: AHRENS MJ BERRY SA WHITLEY CB MARKOWITZ DJ PLANTE RJ TUCHMAN M
Citation: Mj. Ahrens et al., CLINICAL AND BIOCHEMICAL HETEROGENEITY IN FEMALES OF A LARGE PEDIGREEWITH ORNITHINE TRANSCARBAMYLASE DEFICIENCY DUE TO THE R141Q MUTATION (VOL 66, PG 311, 1996), American journal of medical genetics, 71(1), 1997, pp. 125-125
SUBCONJUNCTIVAL-LIMBAL INJECTION OF RETROVIRALLY TRANSDUCED FIBROBLASTS - A POSSIBLE APPROACH FOR GENE DELIVERY TO THE CORNEA
Authors: DJALILIAN AR ARONOVICH EL BRADSHAW JJ CHO WF OBRITSCH WF CHAN CC WHITLEY CB KRACHMER JH HOLLAND EJ
Citation: Ar. Djalilian et al., SUBCONJUNCTIVAL-LIMBAL INJECTION OF RETROVIRALLY TRANSDUCED FIBROBLASTS - A POSSIBLE APPROACH FOR GENE DELIVERY TO THE CORNEA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4411-4411
RETROVIRAL TRANSDUCTION OF PERIPHERAL-BLOOD LEUKOCYTES IN A HOLLOW-FIBER BIOREACTOR
Authors: SHANKAR R WHITLEY CB PAN D BURGER S MCCULLOUGH J STRONCEK D
Citation: R. Shankar et al., RETROVIRAL TRANSDUCTION OF PERIPHERAL-BLOOD LEUKOCYTES IN A HOLLOW-FIBER BIOREACTOR, Transfusion, 37(7), 1997, pp. 685-690
CLINICAL-TRIAL OF GENE-THERAPY FOR A MANNOSE-6-PHOSPHATE RECEPTOR-MEDIATED LYSOSOMAL STORAGE DISEASE, MUCOPOLYSACCHARIDOSIS TYPE-II (HUNTER-SYNDROME)
Authors: WHITLEY CB MCIVOR RS PAN D STRONCEK DF ARONOVICH EL BURGER SR MCCULLOUGH J
Citation: Cb. Whitley et al., CLINICAL-TRIAL OF GENE-THERAPY FOR A MANNOSE-6-PHOSPHATE RECEPTOR-MEDIATED LYSOSOMAL STORAGE DISEASE, MUCOPOLYSACCHARIDOSIS TYPE-II (HUNTER-SYNDROME), American journal of human genetics, 61(4), 1997, pp. 2105-2105
RETROVIRAL-MEDIATED TRANSFER OF THE IDURONATE-2-SULFATASE GENE INTO LYMPHOCYTES FOR TREATMENT OF MILD HUNTER SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE-II)
Authors: WHITLEY CB MCIVOR RS ARONOVICH EL BERRY SA BLAZAR BR BURGER SR KERSEY JH KING RA FARAS AJ LATCHAW RE MCCULLOUGH J PAN D RAMSAY NKC STRONCEK DF
Citation: Cb. Whitley et al., RETROVIRAL-MEDIATED TRANSFER OF THE IDURONATE-2-SULFATASE GENE INTO LYMPHOCYTES FOR TREATMENT OF MILD HUNTER SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE-II), Human gene therapy, 7(4), 1996, pp. 537-549
PRECLINICAL STUDIES OF LYMPHOCYTE GENE-THERAPY FOR MILD HUNTER SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE-II)
Authors: BRAUN SE PAN D ARONOVICH EL JONSSON JJ MCIVOR RS WHITLEY CB
Citation: Se. Braun et al., PRECLINICAL STUDIES OF LYMPHOCYTE GENE-THERAPY FOR MILD HUNTER SYNDROME (MUCOPOLYSACCHARIDOSIS TYPE-II), Human gene therapy, 7(3), 1996, pp. 283-290
CLINICAL AND BIOCHEMICAL HETEROGENEITY IN FEMALES OF A LARGE PEDIGREEWITH ORNITHINE TRANSCARBAMYLASE DEFICIENCY DUE TO THE R141Q MUTATION
Authors: AHRENS MJ BERRY SA WHITLEY CB MARKOWITZ DJ PLANTE RJ TUCHMAN M
Citation: Mj. Ahrens et al., CLINICAL AND BIOCHEMICAL HETEROGENEITY IN FEMALES OF A LARGE PEDIGREEWITH ORNITHINE TRANSCARBAMYLASE DEFICIENCY DUE TO THE R141Q MUTATION, American journal of medical genetics, 66(3), 1996, pp. 311-315
TOPICAL RETROVIRUS GENE-THERAPY FOR SCHEIE KERATOPATHY
Authors: WHITLEY CB ARONOVICH EL PFISTER DR OBRITSCH WF PAN D KRACHMER JH HOLLAND EJ
Citation: Cb. Whitley et al., TOPICAL RETROVIRUS GENE-THERAPY FOR SCHEIE KERATOPATHY, Investigative ophthalmology & visual science, 37(3), 1996, pp. 3124-3124
MOLECULAR-GENETIC DEFECT UNDERLYING ALPHA-L-IDURONIDASE PSEUDODEFICIENCY
Authors: ARONOVICH EL PAN D WHITLEY CB
Citation: El. Aronovich et al., MOLECULAR-GENETIC DEFECT UNDERLYING ALPHA-L-IDURONIDASE PSEUDODEFICIENCY, American journal of human genetics, 58(1), 1996, pp. 75-85
RETROVIRUS PRODUCTION AND TRANSDUCTION OF PERIPHERAL-BLOOD LYMPHOCYTES IN A CLOSED ARTIFICIAL CAPILLARY SYSTEM - AN APPROACH TO LARGE-SCALECELL MANIPULATION FOR CLINICAL GENE-THERAPY
Authors: PAN D SHANKAR R STRONCEK DF MCCULLOUGH J MCIVOR RS WHITLEY CB
Citation: D. Pan et al., RETROVIRUS PRODUCTION AND TRANSDUCTION OF PERIPHERAL-BLOOD LYMPHOCYTES IN A CLOSED ARTIFICIAL CAPILLARY SYSTEM - AN APPROACH TO LARGE-SCALECELL MANIPULATION FOR CLINICAL GENE-THERAPY, Journal of cellular biochemistry, 1995, pp. 412-412
ECHOCARDIOGRAPHIC EVALUATION OF PATIENTS WITH SANFILIPPO-SYNDROME FOLLOWING BONE-MARROW TRANSPLANTATION
Authors: LOHR J BASS JL KRIVIT W WHITLEY CB BRAUNLIN EA
Citation: J. Lohr et al., ECHOCARDIOGRAPHIC EVALUATION OF PATIENTS WITH SANFILIPPO-SYNDROME FOLLOWING BONE-MARROW TRANSPLANTATION, Pediatric research, 37(4), 1995, pp. 150-150
PRECLINICAL STUDIES OF TOPICAL IN-VIVO GENE-THERAPY FOR SCHEIE KERATOPATHY ASSOCIATED WITH MUCOPOLYSACCHARIDOSIS TYPE-I
Authors: ARONOVICH EL PFISTER DR HOLLAND EJ PAN D OBRITSCH W SINCLAIR JM BRADSHAW JJ ANDERSON JA KRACHMER JH WHITLEY CB
Citation: El. Aronovich et al., PRECLINICAL STUDIES OF TOPICAL IN-VIVO GENE-THERAPY FOR SCHEIE KERATOPATHY ASSOCIATED WITH MUCOPOLYSACCHARIDOSIS TYPE-I, American journal of human genetics, 57(4), 1995, pp. 223-223
RETROVIRUS VECTOR STUDIES TOWARD HEMATOPOIETIC STEM-CELL GENE-THERAPYFOR MUCOPOLYSACCHARIDOSIS TYPE-I
Authors: PAN D ARONOVICH EL MCIVOR RS WHITLEY CB
Citation: D. Pan et al., RETROVIRUS VECTOR STUDIES TOWARD HEMATOPOIETIC STEM-CELL GENE-THERAPYFOR MUCOPOLYSACCHARIDOSIS TYPE-I, American journal of human genetics, 57(4), 1995, pp. 1435-1435
MOLECULAR DIAGNOSIS OF MUCOPOLYSACCHARIDOSIS TYPE-II (HUNTER SYNDROME) BY AUTOMATED SEQUENCING AND COMPUTER-ASSISTED INTERPRETATION - TOWARD MUTATION MAPPING OF THE IDURONATE-2-SULFATASE GENE
Authors: JONSSON JJ ARONOVICH EL BRAUN SE WHITLEY CB
Citation: Jj. Jonsson et al., MOLECULAR DIAGNOSIS OF MUCOPOLYSACCHARIDOSIS TYPE-II (HUNTER SYNDROME) BY AUTOMATED SEQUENCING AND COMPUTER-ASSISTED INTERPRETATION - TOWARD MUTATION MAPPING OF THE IDURONATE-2-SULFATASE GENE, American journal of human genetics, 56(3), 1995, pp. 597-607
A NEW MTDNA MUTATION IN THE TRNA(LEU(UUR)) GENE ASSOCIATED WITH MATERNALLY INHERITED CARDIOMYOPATHY
Authors: SILVESTRI G SANTORELLI FM SHANSKE S WHITLEY CB SCHIMMENTI LA SMITH SA DIMAURO S
Citation: G. Silvestri et al., A NEW MTDNA MUTATION IN THE TRNA(LEU(UUR)) GENE ASSOCIATED WITH MATERNALLY INHERITED CARDIOMYOPATHY, Human mutation, 3(1), 1994, pp. 37-43
PRECLINICAL STUDIES OF LYMPHOCYTE GENE-THERAPY FOR HUNTER SYNDROME
Authors: PAN D BRAUN SE JONSSON JJ ARONOVICH EL MCIVOR RS WHITLEY CB
Citation: D. Pan et al., PRECLINICAL STUDIES OF LYMPHOCYTE GENE-THERAPY FOR HUNTER SYNDROME, Journal of cellular biochemistry, 1994, pp. 244-244
POSITIVE NEUROPSYCHOLOGICAL OUTCOME AFTER BONE-MARROW TRANSPLANTATIONIN HURLER-SYNDROME
Authors: SHAPIRO EG LOCKMAN LA BALTHAZOR MJ WHITLEY CB KRIVIT W
Citation: Eg. Shapiro et al., POSITIVE NEUROPSYCHOLOGICAL OUTCOME AFTER BONE-MARROW TRANSPLANTATIONIN HURLER-SYNDROME, Annals of neurology, 36(3), 1994, pp. 491-491
DENSE PERIPHERAL CORNEAL CLOUDING IN SCHEIE SYNDROME
Authors: SUMMERS CG WHITLEY CB HOLLAND EJ PURPLE RL KRIVIT W
Citation: Cg. Summers et al., DENSE PERIPHERAL CORNEAL CLOUDING IN SCHEIE SYNDROME, Cornea, 13(3), 1994, pp. 277-279
LIGHT AND ELECTRON-MICROSCOPIC FEATURES OF THE LIVER IN MUCOPOLYSACCHARIDOSIS
Authors: RESNICK JM WHITLEY CB LEONARD AS KRIVIT W SNOVER DC
Citation: Jm. Resnick et al., LIGHT AND ELECTRON-MICROSCOPIC FEATURES OF THE LIVER IN MUCOPOLYSACCHARIDOSIS, Human pathology, 25(3), 1994, pp. 276-286
NATURE AND RECURRENCE OF AVPR2 MUTATIONS IN X-LINKED NEPHROGENIC DIABETES-INSIPIDUS
Authors: BICHET DG BIRNBAUMER M LONERGAN M ARTHUS MF ROSENTHAL W GOODYER P NIVET H BENOIT S GIAMPIETRO P SIMONETTI S FISH A WHITLEY CB JAEGER P GERTNER J NEW M DIBONA FJ KAPLAN BS ROBERTSON GL HENDY GN FUJIWARA TM MORGAN K
Citation: Dg. Bichet et al., NATURE AND RECURRENCE OF AVPR2 MUTATIONS IN X-LINKED NEPHROGENIC DIABETES-INSIPIDUS, American journal of human genetics, 55(2), 1994, pp. 278-286
CAVEAT TO GENOTYPE-PHENOTYPE CORRELATION IN MUCOPOLYSACCHARIDOSIS TYPE-II - DISCORDANT CLINICAL SEVERITY OF R468W-MUTATIONS AND R468Q-MUTATIONS OF THE IDURONATE-2-SULFATASE GENE
Authors: WHITLEY CB ANDERSON RA ARONOVICH EL CROTTY PL ANYANEYEBOA K RUSSO D WARBURTON D
Citation: Cb. Whitley et al., CAVEAT TO GENOTYPE-PHENOTYPE CORRELATION IN MUCOPOLYSACCHARIDOSIS TYPE-II - DISCORDANT CLINICAL SEVERITY OF R468W-MUTATIONS AND R468Q-MUTATIONS OF THE IDURONATE-2-SULFATASE GENE, Human mutation, 2(3), 1993, pp. 235-237
RETROVIRAL-MEDIATED TRANSFER AND EXPRESSION OF HUMAN IDURONATE-2-SULFATASE CDNA IN LYMPHOID-CELLS - METABOLIC CORRECTION AND CROSS-CORRECTION OF MUCOPOLYSACCHARIDOSIS-II (HUNTER SYNDROME)
Authors: WHITLEY CB BRAUN SE CROTTY PL ANDERSON RA JONSSON JJ MCIVOR RS
Citation: Cb. Whitley et al., RETROVIRAL-MEDIATED TRANSFER AND EXPRESSION OF HUMAN IDURONATE-2-SULFATASE CDNA IN LYMPHOID-CELLS - METABOLIC CORRECTION AND CROSS-CORRECTION OF MUCOPOLYSACCHARIDOSIS-II (HUNTER SYNDROME), Journal of cellular biochemistry, 1993, pp. 234-234
Risultati: 1-25 | 26-31