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Results:
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Results: 20
Authors:
BRADLEY JF
BAKER D
SCHWARTZ ID
ROTHBERG PG
Citation: Jf. Bradley et al., THE IMPORTANCE OF HETERODUPLEXES IN INTERPRETING THE RESULTS OF PCR-RED DIAGNOSTIC ASSAYS - APPLICATION TO THE ANALYSIS OF MUTATIONS IN THESTEROID 21-HYDROXYLASE GENE IN A CASE OF CONGENITAL ADRENAL-HYPERPLASIA, Molecular diagnosis, 3(2), 1998, pp. 119-124
Authors:
SCHWARTZ ID
Citation: Id. Schwartz, HYPONATREMIC SEIZURE IN A CHILD USING DESMOPRESSIN FOR NOCTURNAL ENURESIS, Archives of pediatrics & adolescent medicine, 152(10), 1998, pp. 1037-1038
Authors:
SCHWARTZ ID
Citation: Id. Schwartz, DIFFERENCES IN THE IN-VIVO INSULIN-SECRETION AND SENSITIVITY OF HEALTHY BLACK VERSUS WHITE ADOLESCENTS, The Journal of pediatrics, 130(6), 1997, pp. 1011-1012
Authors:
SCHWARTZ ID
ALON US
Citation: Id. Schwartz et Us. Alon, BARTTER-SYNDROME REVISITED, JN. Journal of nephrology, 9(2), 1996, pp. 81-87
Authors:
SCHWARTZ ID
WARADY BA
REDDIG N
MEEK K
Citation: Id. Schwartz et al., ELEVATED GLYCOSYLATED HEMOGLOBIN IN A PATIENT RECEIVING RECOMBINANT ERYTHROPOIETIN, Pediatric nephrology, 10(6), 1996, pp. 809-810
Authors:
GIEP T
RAIBBLE P
ZUERLEIN T
SCHWARTZ ID
Citation: T. Giep et al., TRIAL OF BECLOMETHASONE DIPROPIONATE BY METERED-DOSE INHALER IN VENTILATOR-DEPENDENT NEONATES LESS-THAN 1500 GRAMS, American journal of perinatology, 13(1), 1996, pp. 5-9
Authors:
SALBERT BA
SCHWARTZ ID
GRUNT JA
Citation: Ba. Salbert et al., SEX REVERSAL IN AN INFANT WITH SMITH-LEMLI-OPITZ SYNDROME, TYPE-II - EVIDENCE FOR 5-ALPHA REDUCTASE DEFICIENCY, Journal of pediatric endocrinology & metabolism, 9(1), 1996, pp. 67-69
Authors:
SCHWARTZ ID
JACOBSON JD
Citation: Id. Schwartz et Jd. Jacobson, AUTOSOMAL RECESSIVE PSEUDOHYPOALDOSTERONISM TYPE-I (PHA-I) WITH CONGENITAL GLAUCOMA AND DIMINISHED IMMUNOGLOBULINS - EXPANDING THE PHENOTYPE, Pediatric research, 39(4), 1996, pp. 577-577
Authors:
SCHWARTZ ID
WARADY BA
HUSSEY LM
Citation: Id. Schwartz et al., GROWTH-HORMONE (GH) THERAPY IN CYSTINOSIS, Pediatric research, 39(4), 1996, pp. 2200-2200
Authors:
SCHWARTZ ID
WARADY BA
REDDIG N
MEEKS K
Citation: Id. Schwartz et al., RECOMBINANT ERYTHROPOIETIN (REPO) INDUCED ELEVATION IN GLYCOSYLATED HEMOGLOBIN (GHB) DUE TO INCREASED SYNTHESIS OF HEMOGLOBIN-F (HGBF) IN END-STAGE RENAL-DISEASE (ESRD), Pediatric research, 39(4), 1996, pp. 2201-2201
Authors:
SCHWARTZ ID
WARADY BA
BUCHANAN CL
REED L
HUSSEY LM
HOWARD CP
HELLERSTEIN S
GRUNT JA
Citation: Id. Schwartz et al., LOW-DOSE GROWTH-HORMONE THERAPY DURING PERITONEAL-DIALYSIS OR FOLLOWING RENAL-TRANSPLANTATION, Pediatric nephrology, 9(3), 1995, pp. 320-324
Authors:
GRUNT JA
SCHWARTZ ID
BUCHANAN C
HOWARD CP
Citation: Ja. Grunt et al., EFFECTS OF LONG-TERM GROWTH-HORMONE RELEASING HORMONE 1-29 IN SIGNIFICANTLY SHORT CHILDREN, Acta paediatrica, 84(6), 1995, pp. 631-633
Authors:
SCHWARTZ ID
ZALLES MC
FOSTER JL
BURRY VF
Citation: Id. Schwartz et al., PITUITARY ABSCESS - AN UNUSUAL PRESENTATION OF ASEPTIC-MENINGITIS, Journal of pediatric endocrinology & metabolism, 8(2), 1995, pp. 141-146
Authors:
SCHWARTZ ID
SCAGLIOTTI D
Citation: Id. Schwartz et D. Scagliotti, VERAPAMIL-INDUCED PRIMARY POLYDIPSIA, Pediatric cardiology, 16(5), 1995, pp. 228-230
Authors:
PASZTOR LM
ROGERS JC
SCHWARTZ ID
HARRIS DJ
Citation: Lm. Pasztor et al., DE-NOVO TRISOMY 6P, American journal of human genetics, 57(4), 1995, pp. 684-684
Authors:
SCHWARTZ ID
HUSSEY LM
GRUNT JA
HOWARD CP
Citation: Id. Schwartz et al., PROLACTINOMA ASSOCIATED WITH TRANSIENT GROWTH-HORMONE DEFICIENCY BUT PERSISTENT GROWTH-RETARDATION, Journal of pediatric endocrinology, 7(1), 1994, pp. 69-73
Authors:
SCHWARTZ ID
FREEMAN AI
GRUNT JA
Citation: Id. Schwartz et al., SERUM CONCENTRATIONS OF ALPHA-FETOPROTEIN IN CHILDREN WITH PRIMARY HYPOTHYROIDISM, Archives of pediatrics & adolescent medicine, 148(2), 1994, pp. 225-227
Authors:
JORGENSEN EV
SCHWARTZ ID
HVIZDALA E
BARBOSA J
PHUPHANICH S
SHULMAN DI
ROOT AW
ESTRADA J
HU CS
BERCU BB
Citation: Ev. Jorgensen et al., NEUROTRANSMITTER CONTROL OF GROWTH-HORMONE SECRETION IN CHILDREN AFTER CRANIAL RADIATION-THERAPY, Journal of pediatric endocrinology, 6(2), 1993, pp. 131-142
Authors:
PASZTOR LM
SCHWARTZ ID
Citation: Lm. Pasztor et Id. Schwartz, FAMILIAL TURNER VARIANT WITH A DUPLICATED DELETED X-CHROMOSOME, Cytogenetics and cell genetics, 63(4), 1993, pp. 252-252
Authors:
SCHWARTZ ID
MOU SM
ZWICK DL
GILBERTBARNESS E
Citation: Id. Schwartz et al., PATHOLOGICAL CASE OF THE MONTH - OVARIAN STROMAL HYPERTHECOSIS, American journal of diseases of children [1960], 147(5), 1993, pp. 591-592
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