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Results: 1-25 | 26-47
Results: 1-25/47
HUMAN-COMPLEMENT FACTOR-H DEFICIENCY ASSOCIATED WITH HEMOLYTIC-UREMICSYNDROME
Authors: ROUGIER N KAZATCHKINE MD ROUGIER JP FREMEAUXBACCHI V BLOUIN J DESCHENES C SOTO B BAUDOUIN V PAUTARD B PROESMANS W WEISS E WEISS L
Citation: N. Rougier et al., HUMAN-COMPLEMENT FACTOR-H DEFICIENCY ASSOCIATED WITH HEMOLYTIC-UREMICSYNDROME, Journal of the American Society of Nephrology, 9(12), 1998, pp. 2318-2326
ASK THE EXPERT
Authors: PROESMANS W
Citation: W. Proesmans, ASK THE EXPERT, Pediatric nephrology, 12(8), 1998, pp. 698-699
NEONATAL BARTTER-SYNDROME - SPONTANEOUS RESOLUTION OF ALL SIGNS AND SYMPTOMS
Authors: REINALTER S DEVLIEGER H PROESMANS W
Citation: S. Reinalter et al., NEONATAL BARTTER-SYNDROME - SPONTANEOUS RESOLUTION OF ALL SIGNS AND SYMPTOMS, Pediatric nephrology, 12(3), 1998, pp. 186-188
CHRONIC-RENAL-FAILURE IN INFANTS - EFFECT OF STRICT CONSERVATIVE TREATMENT ON GROWTH
Authors: VANDYCK M SIDLER S PROESMANS W
Citation: M. Vandyck et al., CHRONIC-RENAL-FAILURE IN INFANTS - EFFECT OF STRICT CONSERVATIVE TREATMENT ON GROWTH, European journal of pediatrics, 157(9), 1998, pp. 759-762
MULTICYSTIC KIDNEY DYSPLASIA - A PROSPECTIVE-STUDY ON THE NATURAL-HISTORY OF THE AFFECTED AND THE CONTRALATERAL KIDNEY
Authors: HEYMANS C BREYSEM L PROESMANS W
Citation: C. Heymans et al., MULTICYSTIC KIDNEY DYSPLASIA - A PROSPECTIVE-STUDY ON THE NATURAL-HISTORY OF THE AFFECTED AND THE CONTRALATERAL KIDNEY, European journal of pediatrics, 157(8), 1998, pp. 673-675
VESICOURETERAL REFLUX - A GENETIC CONDITION
Authors: DEVRIENDT K GROENEN P VANESCH H VANDIJCK M VANDEVEN W FRYNS JP PROESMANS W
Citation: K. Devriendt et al., VESICOURETERAL REFLUX - A GENETIC CONDITION, European journal of pediatrics, 157(4), 1998, pp. 265-271
RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS IN A BOY WITH HYPOCOMPLEMENTEMIC URTICARIAL VASCULITIS
Authors: RENARD M WOUTERS C PROESMANS W
Citation: M. Renard et al., RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS IN A BOY WITH HYPOCOMPLEMENTEMIC URTICARIAL VASCULITIS, European journal of pediatrics, 157(3), 1998, pp. 243-245
3-YEAR-OLD GIRL WITH RICKETS AND HEPATOMEGALY
Authors: PROESMANS W DECOSTER J BREYSEM L JAEKEN J
Citation: W. Proesmans et al., 3-YEAR-OLD GIRL WITH RICKETS AND HEPATOMEGALY, European journal of pediatrics, 157(1), 1998, pp. 83-84
ACTIVATION OF BOTH COAGULATION AND FIBRINOLYSIS IN CHILDHOOD HEMOLYTIC-UREMIC SYNDROME
Authors: VANGEET C PROESMANS W ARNOUT J VERMYLEN J DECLERCK PJ
Citation: C. Vangeet et al., ACTIVATION OF BOTH COAGULATION AND FIBRINOLYSIS IN CHILDHOOD HEMOLYTIC-UREMIC SYNDROME, Kidney international, 54(4), 1998, pp. 1324-1330
MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997)
Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPWJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997), Human molecular genetics, 6(4), 1997, pp. 650-650
MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 6(1), 1997, pp. 17-26
BARTTER-SYNDROME AND ITS NEONATAL VARIANT
Authors: PROESMANS W
Citation: W. Proesmans, BARTTER-SYNDROME AND ITS NEONATAL VARIANT, European journal of pediatrics, 156(9), 1997, pp. 669-679
PRADER-WILLI-SYNDROME IN A CHILD WITH MOSAIC TRISOMY-15 AND MOSAIC TRIPLO-X - A MOLECULAR ANALYSIS
Authors: DEVRIENDT K MATTHIJS G CLAES S LEGIUS E PROESMANS W CASSIMAN JJ FRYNS JP
Citation: K. Devriendt et al., PRADER-WILLI-SYNDROME IN A CHILD WITH MOSAIC TRISOMY-15 AND MOSAIC TRIPLO-X - A MOLECULAR ANALYSIS, Journal of Medical Genetics, 34(4), 1997, pp. 318-322
FURTHER DELINEATION OF RENAL-COLOBOMA SYNDROME IN PATIENTS WITH EXTREME VARIABILITY OF PHENOTYPE AND IDENTICAL PAX2 MUTATIONS
Authors: SCHIMMENTI LA CUNLIFFE HE MCNOE LA WARD TA FRENCH MC SHIM HH ZHANG YH PROESMANS W LEYS A BYERLY KA BRADDOCK SR MASUNO M IMAIZUMI K DEVRIENDT K ECCLES MR
Citation: La. Schimmenti et al., FURTHER DELINEATION OF RENAL-COLOBOMA SYNDROME IN PATIENTS WITH EXTREME VARIABILITY OF PHENOTYPE AND IDENTICAL PAX2 MUTATIONS, American journal of human genetics, 60(4), 1997, pp. 869-878
TYPICAL AND ATYPICAL HEMOLYTIC-UREMIC SYNDROME
Authors: PROESMANS W
Citation: W. Proesmans, TYPICAL AND ATYPICAL HEMOLYTIC-UREMIC SYNDROME, Kidney & blood pressure research, 19(3-4), 1996, pp. 205-208
LONG-TERM THERAPY WITH ENALAPRIL IN PATIENTS WITH NEPHROTIC-RANGE PROTEINURIA
Authors: PROESMANS W VANWAMBEKE I VANDYCK M
Citation: W. Proesmans et al., LONG-TERM THERAPY WITH ENALAPRIL IN PATIENTS WITH NEPHROTIC-RANGE PROTEINURIA, Pediatric nephrology, 10(5), 1996, pp. 587-589
HEMOLYTIC-UREMIC SYNDROME SUPERIMPOSED ON ACUTE GLOMERULONEPHRITIS
Authors: PROESMANS W
Citation: W. Proesmans, HEMOLYTIC-UREMIC SYNDROME SUPERIMPOSED ON ACUTE GLOMERULONEPHRITIS, Pediatric nephrology, 10(5), 1996, pp. 679-679
UNTITLED
Authors: PROESMANS W
Citation: W. Proesmans, UNTITLED, Pediatric nephrology, 10(4), 1996, pp. 411-411
HYPERCALCEMIA, HYPERCALCIURIA AND NEPHROCALCINOSIS IN DOWN-SYNDROME
Authors: PROESMANS W
Citation: W. Proesmans, HYPERCALCEMIA, HYPERCALCIURIA AND NEPHROCALCINOSIS IN DOWN-SYNDROME, Pediatric nephrology, 10(4), 1996, pp. 543-544
VEROCYTOTOXIN-PRODUCING ESCHERICHIA-COLI INFECTION IN HEMOLYTIC-UREMIC SYNDROME IN PART OF WESTERN-EUROPE
Authors: VANDEKAR NCAJ ROELOFS HGR MUYTJENS HL TOLBOOM JJM ROTH B PROESMANS W WOLFF ED KARMALI MA CHART H MONNENS LAH
Citation: Ncaj. Vandekar et al., VEROCYTOTOXIN-PRODUCING ESCHERICHIA-COLI INFECTION IN HEMOLYTIC-UREMIC SYNDROME IN PART OF WESTERN-EUROPE, European journal of pediatrics, 155(7), 1996, pp. 592-595
CASE-OF-THE-MONTH - A GIRL WITH ULLRICH-TURNER SYNDROME, NEPHROLITHIASIS AND HYPERCALCEMIA - DIAGNOSIS - PARATHYROID ADENOMA IN ULLRICH-TURNER SYNDROME
Authors: FRANCOIS I PROESMANS W DEZEGHER F
Citation: I. Francois et al., CASE-OF-THE-MONTH - A GIRL WITH ULLRICH-TURNER SYNDROME, NEPHROLITHIASIS AND HYPERCALCEMIA - DIAGNOSIS - PARATHYROID ADENOMA IN ULLRICH-TURNER SYNDROME, European journal of pediatrics, 155(7), 1996, pp. 615-616
PAUCITY OF INTRAHEPATIC BILE-DUCTS, SOLITARY KIDNEY AND ATROPHIC PANCREAS WITH DIABETES-MELLITUS - ATYPICAL ALAGILLE SYNDROME
Authors: DEVRIENDT K DOOMS L PROESMANS W DEZEGHER F DESMET V EGGERMONT E
Citation: K. Devriendt et al., PAUCITY OF INTRAHEPATIC BILE-DUCTS, SOLITARY KIDNEY AND ATROPHIC PANCREAS WITH DIABETES-MELLITUS - ATYPICAL ALAGILLE SYNDROME, European journal of pediatrics, 155(2), 1996, pp. 87-90
ALPORT SYNDROME - CLINICAL-EXPERIENCE WITH 21 PEDIATRIC-PATIENTS
Authors: BARTEN S PROESMANS W
Citation: S. Barten et W. Proesmans, ALPORT SYNDROME - CLINICAL-EXPERIENCE WITH 21 PEDIATRIC-PATIENTS, European journal of pediatrics, 155(1), 1996, pp. 49-52
LOW-MOLECULAR-WEIGHT HEPARIN FOR ANTICOAGULATION DURING HEMODIALYSIS IN CHILDREN - A PRELIMINARY-STUDY
Authors: VANBILJON I VANDAMMELOMBAERTS R DEMOL A VANGEET C PROESMANS W ARNOUT J
Citation: I. Vanbiljon et al., LOW-MOLECULAR-WEIGHT HEPARIN FOR ANTICOAGULATION DURING HEMODIALYSIS IN CHILDREN - A PRELIMINARY-STUDY, European journal of pediatrics, 155(1), 1996, pp. 70-70
TC-99M DIMERCAPTOSUCCINATE SCINTIGRAPHY IN PEDIATRIC VESICOURETERAL REFLUX
Authors: SCHIEPERS C MESOTTEN L PROESMANS W VEREECKEN R VERBRUGGEN A DEROO M
Citation: C. Schiepers et al., TC-99M DIMERCAPTOSUCCINATE SCINTIGRAPHY IN PEDIATRIC VESICOURETERAL REFLUX, Radiology, 201, 1996, pp. 1661-1661
Risultati: 1-25 | 26-47