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Results:
1-12
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Results: 12
Authors:
BECKER JA
VLACH J
RABEN N
NAGARAJU K
ADAMS EM
HERMANS MM
REUSER AJJ
BROOKS SS
TIFFT CJ
HIRSCHHORN R
HUIE ML
NICOLINO M
PLOTZ PH
Citation: Ja. Becker et al., THE AFRICAN ORIGIN OF THE COMMON MUTATION IN AFRICAN-AMERICAN PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-II, American journal of human genetics, 62(4), 1998, pp. 991-994
Authors:
NICOLINO M
Citation: M. Nicolino, DIFFERENT ANIMAL-MODELS FOR GLYCOGENOSIS TYPE-II, MS. Medecine sciences, 14(6-7), 1998, pp. 795-795
Authors:
CHATELAIN PG
NICOLINO M
CLARIS O
SALLE B
CHAUSSAIN JL
Citation: Pg. Chatelain et al., MULTIPLE HORMONE RESISTANCE IN SHORT CHILDREN BORN WITH INTRAUTERINE GROWTH-RETARDATION, Hormone research, 49, 1998, pp. 20-22
Authors:
NICOLINO M
Citation: M. Nicolino, POTASSIUM CHANNELS PLAY A KEY ROLE IN HYP ERINSULINISM OF THE NEONATE, MS. Medecine sciences, 13(2), 1997, pp. 276-277
Authors:
LAFORET P
NICOLINO M
EYMARD B
PUECH JP
CAILLAUD C
POENARU L
FARDEAU M
Citation: P. Laforet et al., GENOTYPE-PHENOTYPE CORRELATION IN JUVENILE AND ADULT-ONSET ACID MALTASE DEFICIENCY, Neurology, 48(3), 1997, pp. 5114-5114
Authors:
NICOLINO M
FERLIN T
FOREST M
GODINOT C
CARRIER H
DAVID M
CHATELAIN P
MOUSSON B
Citation: M. Nicolino et al., IDENTIFICATION OF A LARGE-SCALE MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID DELETION IN ENDOCRINOPATHIES AND DEAFNESS - REPORT OF 2 UNRELATED CASESWITH DIABETES-MELLITUS AND ADRENAL INSUFFICIENCY, RESPECTIVELY, The Journal of clinical endocrinology and metabolism, 82(9), 1997, pp. 3063-3067
Authors:
NICOLINO M
PUECH JP
LETOURNEUR F
FARDEAU M
KAHN A
POENARU L
Citation: M. Nicolino et al., GLYCOGEN-STORAGE-DISEASE TYPE-II (ACID MALTASE DEFICIENCY) - IDENTIFICATION OF A NOVEL SMALL DELETION (DELCC482+483) IN FRENCH PATIENTS, Biochemical and biophysical research communications, 235(1), 1997, pp. 138-141
Authors:
AMATI P
CHOMEL JC
KITZIS A
BONNEAU D
NICOLINO M
Citation: P. Amati et al., GENE FOR PREMATURE OVARIAN FAILURE ASSOCI ATED WITH EYELID MALFORMATION MAPS TO CHROMOSOME 3Q22-Q23, MS. Medecine sciences, 12(4), 1996, pp. 539-539
Authors:
NICOLINO M
Citation: M. Nicolino, FAMILIAL BLEPHAROPHIMOSIS AND OVARIAN DYS GENESIS MAP TOGETHER TO CHROMOSOME 3Q23, MS. Medecine sciences, 12(1), 1996, pp. 108-109
Authors:
NICOLINO M
BOST M
DAVID M
CHAUSSAIN JL
Citation: M. Nicolino et al., FAMILIAL BLEPHAROPHIMOSIS - AN UNCOMMON MARKER OF OVARIAN DYSGENESIS, Journal of pediatric endocrinology & metabolism, 8(2), 1995, pp. 127-133
Authors:
DAVID M
SEMPE M
BLANC M
NICOLINO M
FOREST MG
MOREL Y
Citation: M. David et al., FINAL HEIGHT ATTAINED BY 69 SUBJECTS WITH CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY, Archives de pediatrie, 1(4), 1994, pp. 363-367
Authors:
CHATELAIN PG
AVALLET MO
NICOLINO M
LEJEUNE H
CLARK A
CHUZEL F
PENHOAT A
SAEZ JM
Citation: Pg. Chatelain et al., INSULIN-LIKE GROWTH-FACTOR-I ACTIONS ON STEROIDOGENESIS, Acta paediatrica, 83, 1994, pp. 176-177
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