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Results: 1-10 |
Results: 10
IDIOPATHIC NEPHROTIC SYNDROME AND HEXADACTYLY IN 2 BROTHERS
Authors: MALLMANN R
Citation: R. Mallmann, IDIOPATHIC NEPHROTIC SYNDROME AND HEXADACTYLY IN 2 BROTHERS, Pediatric nephrology, 12(5), 1998, pp. 417-419
A GIRL WITH CONGENITAL ADRENAL-HYPERPLASIA AND RECURRENT ABDOMINAL-PAIN
Authors: MALLMANN R KANIA U ROLLMANN O KNOPFLE G
Citation: R. Mallmann et al., A GIRL WITH CONGENITAL ADRENAL-HYPERPLASIA AND RECURRENT ABDOMINAL-PAIN, European journal of pediatrics, 156(11), 1997, pp. 889-890
PHENYLALANINE-HYDROXYLASE DEFICIENCY IN A POPULATION IN GERMANY - MUTATIONAL PROFILE AND 9 NOVEL MUTATIONS
Authors: GULDBERG P MALLMANN R HENRIKSEN KF GUTTLER F
Citation: P. Guldberg et al., PHENYLALANINE-HYDROXYLASE DEFICIENCY IN A POPULATION IN GERMANY - MUTATIONAL PROFILE AND 9 NOVEL MUTATIONS, Human mutation, 8(3), 1996, pp. 276-279
OUTCOME OF IDIOPATHIC MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS IN CHILDREN
Authors: SCHWERTZ R DEJONG R GRETZ N KIRSCHFINK M ANDERS D SCHARER K VANACKER K VERPOOTEN GA SCHULZ W JANSSEN J EGLI F KISS D LENNERT T MALLMANN R WEBER JP BACHMANN HJ DEBUSMANN ER OLBING J DIPPELL J SCHINDERA F SCHOLLMEYER P ZIMMERHACKL LB BLAKER F MULLERWIEFEL DE BRODEHL J KROHN HP WINGEN AM KEHRBERG H BEETZ R SCHULTEWISSERMANN H MONNENS L WALB D ROTHER U THOENES W ASSMANN K WALDHERR R
Citation: R. Schwertz et al., OUTCOME OF IDIOPATHIC MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS IN CHILDREN, Acta paediatrica, 85(3), 1996, pp. 308-312
SCUTULAR FAVUS-LIKE TINEA-CRURIS ET PEDIS IN A PATIENT WITH AIDS
Authors: BAKOS L BONAMIGO RR PISANI AC MARIANTE JC MALLMANN R
Citation: L. Bakos et al., SCUTULAR FAVUS-LIKE TINEA-CRURIS ET PEDIS IN A PATIENT WITH AIDS, Journal of the American Academy of Dermatology, 34(6), 1996, pp. 1086-1087
NORMAL FIBRINOLYTIC RESPONSES TO 1-DESAMINO-8-D-ARGININE VASOPRESSIN IN PATIENTS WITH NEPHROGENIC DIABETES-INSIPIDUS CAUSED BY MUTATIONS INTHE AQUAPORIN-2 GENE
Authors: VANLIEBURG AF KNOERS VVAM MALLMANN R PROESMANS W VANDENHEUVEL LPWJ MONNENS LAH
Citation: Af. Vanlieburg et al., NORMAL FIBRINOLYTIC RESPONSES TO 1-DESAMINO-8-D-ARGININE VASOPRESSIN IN PATIENTS WITH NEPHROGENIC DIABETES-INSIPIDUS CAUSED BY MUTATIONS INTHE AQUAPORIN-2 GENE, Nephron, 72(4), 1996, pp. 544-546
IN-VITRO SCREENING FOR ALLERGIES WITH THE PHARMACIA CAP IGE TEST, THESX1-TEST FOR INHALATIVE ALLERGENS, AND THE FX5 TEST FOR NUTRITIVE ALLERGENS - THE INCIDENCE OF ATOPIA IN CHILDREN
Authors: LIAPPIS N STARKE A MALLMANN R
Citation: N. Liappis et al., IN-VITRO SCREENING FOR ALLERGIES WITH THE PHARMACIA CAP IGE TEST, THESX1-TEST FOR INHALATIVE ALLERGENS, AND THE FX5 TEST FOR NUTRITIVE ALLERGENS - THE INCIDENCE OF ATOPIA IN CHILDREN, Monatsschrift fur Kinderheilkunde, 144(3), 1996, pp. 271-274
LICH-GREGOIR ANTIREFLUX PROCEDURE - INDICATIONS AND RESULTS WITH 283 VESICOURETERAL UNITS
Authors: HEIMBACH D BRUHL P MALLMANN R
Citation: D. Heimbach et al., LICH-GREGOIR ANTIREFLUX PROCEDURE - INDICATIONS AND RESULTS WITH 283 VESICOURETERAL UNITS, Scandinavian journal of urology and nephrology, 29(3), 1995, pp. 311-316
IDENTIFICATION OF A 7-BASEPAIR DELETION IN THE ADENINE PHOSPHORIBOSYL-TRANSFERASE GENE AS A CAUSE OF 2,8-DIHYDROXYADENINE UROLITHIASIS
Authors: BYE S MALLMANN R DULEY J SIMMONDS HA CHEN J TISCHFIELD JA SAHOTA A
Citation: S. Bye et al., IDENTIFICATION OF A 7-BASEPAIR DELETION IN THE ADENINE PHOSPHORIBOSYL-TRANSFERASE GENE AS A CAUSE OF 2,8-DIHYDROXYADENINE UROLITHIASIS, The Clinical investigator, 72(7), 1994, pp. 550-553
PATIENTS WITH AUTOSOMAL NEPHROGENIC DIABETES-INSIPIDUS HOMOZYGOUS FORMUTATIONS IN THE AQUAPORIN-2 WATER-CHANNEL GENE
Authors: VANLIEBURG AF VERDIJK MAJ KNOERS VVAM VANESSEN AJ PROESMANS W MALLMANN R MONNENS LAH VANOOST BA VANOS CH DEEN PMT
Citation: Af. Vanlieburg et al., PATIENTS WITH AUTOSOMAL NEPHROGENIC DIABETES-INSIPIDUS HOMOZYGOUS FORMUTATIONS IN THE AQUAPORIN-2 WATER-CHANNEL GENE, American journal of human genetics, 55(4), 1994, pp. 648-652
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