AAAAAA

   
Results: 1-9 |
Results: 9
TREATMENT OF SMITH-LEMLI-OPITZ SYNDROME - RESULTS OF A MULTICENTER TRIAL
Authors: IRONS M ELIAS ER ABUELO D BULL MJ GREENE CL JOHNSON VP KEPPEN L SCHANEN C TINT GS SALEN G
Citation: M. Irons et al., TREATMENT OF SMITH-LEMLI-OPITZ SYNDROME - RESULTS OF A MULTICENTER TRIAL, American journal of medical genetics, 68(3), 1997, pp. 311-314
CATASTROPHIC METABOLIC ENCEPHALOPATHIES IN THE NEWBORN PERIOD - EVALUATION AND MANAGEMENT
Authors: GREENE CL GOODMAN SI
Citation: Cl. Greene et Si. Goodman, CATASTROPHIC METABOLIC ENCEPHALOPATHIES IN THE NEWBORN PERIOD - EVALUATION AND MANAGEMENT, Clinics in perinatology, 24(4), 1997, pp. 773
NOVEL MUTATIONS IN THE METHIONINE ADENOSYLTRANSFERASE 1A GENE THAT CAUSE ISOLATED PERSISTENT HYPERMETHIONINEMIA
Authors: CHAMBERLIN ME UBAGAI T MUDD SH PAO VY NGUYEN TK GREENE CL THOMAS JA FREEHAUF C CHOU JY
Citation: Me. Chamberlin et al., NOVEL MUTATIONS IN THE METHIONINE ADENOSYLTRANSFERASE 1A GENE THAT CAUSE ISOLATED PERSISTENT HYPERMETHIONINEMIA, American journal of human genetics, 61(4), 1997, pp. 1448-1448
RADIOCEPHALOMETRIC EVALUATION OF A FAMILY WITH MANDIBULOFACIAL DYSOSTOSIS
Authors: BHATIA S BLOCK MS HOFFMAN DR LANCASTER D GREENE CL
Citation: S. Bhatia et al., RADIOCEPHALOMETRIC EVALUATION OF A FAMILY WITH MANDIBULOFACIAL DYSOSTOSIS, American journal of orthodontics and dentofacial orthopedics, 110(6), 1996, pp. 618-623
TREATMENT OF SMITH-LEMLI-OPITZ SYNDROME (SLOS) - RESULTS OF A MULTICENTER TRIAL
Authors: IRONS M ELIAS ER ABUELO D BULL MJ GREENE CL JOHNSON VP KEPPEN L SCHANEN C TINT GS SALEN G
Citation: M. Irons et al., TREATMENT OF SMITH-LEMLI-OPITZ SYNDROME (SLOS) - RESULTS OF A MULTICENTER TRIAL, American journal of human genetics, 57(4), 1995, pp. 87-87
COGNITIVE-DEVELOPMENT AMONG CHILDREN WITH EARLY-TREATED PHENYLKETONURIA
Authors: MAZZOCCO MMM NORD AM VANDOORNINCK W GREENE CL KOVAR CG PENNINGTON BF
Citation: Mmm. Mazzocco et al., COGNITIVE-DEVELOPMENT AMONG CHILDREN WITH EARLY-TREATED PHENYLKETONURIA, Developmental neuropsychology, 10(2), 1994, pp. 133-151
INTRAFAMILIAL VARIABILITY IN HURLER-SYNDROME AND SANFILIPPO SYNDROME TYPE-A - IMPLICATIONS FOR EVALUATION OF NEW THERAPIES
Authors: MCDOWELL GA COWAN TM BLITZER MG GREENE CL
Citation: Ga. Mcdowell et al., INTRAFAMILIAL VARIABILITY IN HURLER-SYNDROME AND SANFILIPPO SYNDROME TYPE-A - IMPLICATIONS FOR EVALUATION OF NEW THERAPIES, American journal of medical genetics, 47(7), 1993, pp. 1092-1095
MOLYBDENUM COFACTOR DEFICIENCY
Authors: ARNOLD GL GREENE CL STOUT JP GOODMAN SI
Citation: Gl. Arnold et al., MOLYBDENUM COFACTOR DEFICIENCY, The Journal of pediatrics, 123(4), 1993, pp. 595-598
MUTATION IN THE 4A-CARBINOLAMINE DEHYDRATASE GENE LEADS TO MILD HYPERPHENYLALANINEMIA WITH DEFECTIVE COFACTOR METABOLISM
Authors: CITRON BA KAUFMAN S MILSTIEN S NAYLOR EW GREENE CL DAVIS MD
Citation: Ba. Citron et al., MUTATION IN THE 4A-CARBINOLAMINE DEHYDRATASE GENE LEADS TO MILD HYPERPHENYLALANINEMIA WITH DEFECTIVE COFACTOR METABOLISM, American journal of human genetics, 53(3), 1993, pp. 768-774
Risultati: 1-9 |