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Results:
1-7
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Results: 7
Authors:
AGGIO MC
FERNANDEZ VV
CHAMOLES N
Citation: Mc. Aggio et al., DEMOGRAPHIC AND CLINICAL ASPECTS OF TYPE-1 GAUCHER-DISEASE (GD) IN ARGENTINA, British Journal of Haematology, 102(1), 1998, pp. 296-296
Authors:
ANDRESEN BS
BROSS P
UDVARI S
KIRK J
GRAY G
KMOCH S
CHAMOLES N
KNUDSEN I
WINTER V
WILCKEN B
YOKOTA I
HART K
PACKMAN S
HARPEY JP
SAUDUBRAY JM
HALE DE
BOLUND L
KOLVRAA S
GREGERSEN N
Citation: Bs. Andresen et al., THE MOLECULAR-BASIS OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY IN COMPOUND HETEROZYGOUS PATIENTS - IS THERE CORRELATION BETWEEN GENOTYPE AND PHENOTYPE, Human molecular genetics, 6(5), 1997, pp. 695-707
Authors:
BARANZINI SE
DELREY G
NIGRO N
SZIJAN I
CHAMOLES N
CRESTO JC
Citation: Se. Baranzini et al., PATIENT WITH AN XP21 CONTIGUOUS GENE DELETION SYNDROME IN ASSOCIATIONWITH AGENESIS OF THE CORPUS-CALLOSUM, American journal of medical genetics, 70(3), 1997, pp. 216-221
Authors:
CONSALVO D
VILLEGAS F
VILLA AM
KOHLER G
MOLINA H
BENCHUGA E
CHAMOLES N
SANZ OP
SICA REP
Citation: D. Consalvo et al., SEVERE CARDIAC-FAILURE IN KEARNS-SAYRE-SY NDROME, Medicina, 57(1), 1997, pp. 67-71
Authors:
CRESTO JC
ABDENUR JE
CHAMOLES N
BRESCIANI P
RUIZ M
MASSA B
CAMBEROS MC
BASABE JC
Citation: Jc. Cresto et al., AUTOIMMUNE HYPOGLYCEMIA SYNDROME DUE TO S PECIFIC ANTI-HUMAN INSULIN-ANTIBODIES, Medicina, 56(3), 1996, pp. 279-283
Authors:
FERRARO SM
CHAMOLES N
SCHENONE JL
FUERTES A
GLANCSZPIGEL R
Citation: Sm. Ferraro et al., OXCARBAZEPINE - PREDICTIVE SERUM CONCENTRATIONS - STUDY OF 153 PATIENTS, Epilepsia, 36, 1995, pp. 161-161
Authors:
CATURELLJ SRM
FRAGA AR
PASCUALINI T
RUIZ S
CHAMOLES N
DAGOSTINO D
Citation: Srm. Caturellj et al., TYROSINEMIA TYPE-I - RESOLUTION OF THE METABOLIC ABNORMALITIES AND INCREASED GROWTH FOLLOWING LIVER-TRANSPLANTATION, Pediatric research, 33(6), 1993, pp. 662-662
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1-7
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