AAAAAA

   
Results: 1-25 | 26-29
Results: 1-25/29

Authors: KOHLENDORFER U KIECHL S SPERL W
Citation: U. Kohlendorfer et al., SUDDEN-INFANT-DEATH-SYNDROME - RISK FACTOR PROFILES FOR DISTINCT SUBGROUPS, American journal of epidemiology, 147(10), 1998, pp. 960-968

Authors: WYSS M FELBER S SKLADAL D KOLLER A KREMSER C SPERL W
Citation: M. Wyss et al., THE THERAPEUTIC POTENTIAL OF ORAL CREATINE SUPPLEMENTATION IN MUSCLE DISEASE, Medical hypotheses, 51(4), 1998, pp. 333-336

Authors: STEICHENGERSDORF E GASSNER I UNSINN K SPERL W
Citation: E. Steichengersdorf et al., PERSISTENT HYPERPLASTIC PRIMARY VITREOUS IN A FAMILY WITH OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME, Clinical dysmorphology, 6(2), 1997, pp. 171-176

Authors: KOHLENDORFER U HABERLANDT E KIECHL S SPERL W
Citation: U. Kohlendorfer et al., PRE-NATAL AND POSTNATAL MEDICAL-CARE AND RISK OF SUDDEN-INFANT-DEATH-SYNDROME, Acta paediatrica, 86(6), 1997, pp. 600-603

Authors: SPERL W GEIGER R LEHNERT W RHEAD W
Citation: W. Sperl et al., STRIDOR AS THE MAJOR PRESENTING SYMPTOM IN RIBOFLAVIN-RESPONSIVE MULTIPLE ACYL-COA DEHYDROGENATION DEFICIENCY, European journal of pediatrics, 156(10), 1997, pp. 800-802

Authors: SPERL W SKLADAL D GNAIGER E WYSS M MAYR U HAGER J GELLERICH FN
Citation: W. Sperl et al., HIGH-RESOLUTION RESPIROMETRY OF PERMEABILIZED SKELETAL-MUSCLE FIBERS IN THE DIAGNOSIS OF NEUROMUSCULAR DISORDERS, Molecular and cellular biochemistry, 174(1-2), 1997, pp. 71-78

Authors: SPERL W FELBER S SKLADAL D WERMUTH B
Citation: W. Sperl et al., METABOLIC STROKE IN CARBAMYL-PHOSPHATE SYNTHETASE DEFICIENCY, Neuropediatrics, 28(4), 1997, pp. 229-234

Authors: DECSI T SPERL W KOLETZKO B
Citation: T. Decsi et al., ESSENTIAL FATTY-ACIDS IN CLINICALLY STABLE CHILDREN WITH PROPIONIC ACIDEMIA, Journal of inherited metabolic disease, 20(6), 1997, pp. 778-782

Authors: SEWELL AC HERWIG J BOHLES HJ SPERL W
Citation: Ac. Sewell et al., MITOCHONDRIAL RESPIRATORY-CHAIN SUCCINATE-CYTOCHROME-C OXIDOREDUCTASEDEFICIENCY AND HEPATIC CIRRHOSIS, Journal of inherited metabolic disease, 20(6), 1997, pp. 837-838

Authors: SPERL W
Citation: W. Sperl, DIAGNOSIS AND THERAPY OF MITOCHONDRIOPATH IES, Wiener Klinische Wochenschrift, 109(3), 1997, pp. 93-99

Authors: SEWELL AC SPERL W HERWIG J BOHLES HJ
Citation: Ac. Sewell et al., CIRRHOSIS IN A CHILD WITH DEFICIENCY OF MITOCHONDRIAL RESPIRATORY-CHAIN SUCCINATE CYTOCHROME-C OXIDOREDUCTASE, The Journal of pediatrics, 131(1), 1997, pp. 166-168

Authors: HENRY H TISSOT JD MESSERLI B MARKERT M MUNTAU A SKLADAL D SPERL W JAEKEN J WEIDINGER S HEYNE K BACHMANN C
Citation: H. Henry et al., MICROHETEROGENEITY OF SERUM GLYCOPROTEINS AND THEIR LIVER PRECURSORS IN PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I -APPARENT DEFICIENCIES IN CLUSTERIN AND SERUM AMYLOID-P, The Journal of laboratory and clinical medicine, 129(4), 1997, pp. 412-421

Authors: VANDERVEERE CN SINAASAPPEL M MCDONAGH AF ROSENTHAL P LABRUNE P ODIEVRE M FEVERY J OTTE JB MCCLEAN P BURK G MASAKOWSKI V SPERL W MOWAT AP VERGANI CM HELLER K WILSON JP SHEPHERD R JANSEN PLM
Citation: Cn. Vanderveere et al., CURRENT THERAPY FOR CRIGLER-NAJJAR SYNDROME TYPE-1 - REPORT OF A WORLD REGISTRY, Hepatology, 24(2), 1996, pp. 311-315

Authors: SKLADAL D SPERL W HENRY H BACHMANN C
Citation: D. Skladal et al., CONGENITAL CATARACT AND FAMILIAL BRACHYDACTYLY IN CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, Journal of inherited metabolic disease, 19(2), 1996, pp. 251-252

Authors: BITTNER RE SHORNY S FERLINGS R SPERL W KRESS W MULLER CR CREMER M LEGER JJ VOIT T
Citation: Re. Bittner et al., SARCOLEMMAL EXPRESSION OF DYSTROPHIN C-TERMINUS BUT REDUCED EXPRESSION OF 6Q-DYSTROPHIN-RELATED PROTEIN IN 2 DMD PATIENTS WITH LARGE DELETIONS OF THE DYSTROPHIN GENE, Neuromuscular disorders, 5(2), 1995, pp. 81-92

Authors: SIMMA B MEISTER B DEUTSCH J SPERL W FEND F OFNER D MARGREITER R VOGEL W
Citation: B. Simma et al., FULMINANT HEPATIC-FAILURE IN A CHILD AS A POTENTIAL ADVERSE EFFECT OFTRIMETHOPRIM-SULFAMETHOXAZOLE, European journal of pediatrics, 154(7), 1995, pp. 530-533

Authors: SPERL W STUPPNER H GASSNER I JUDMAIER W DIETZE O VOGEL W
Citation: W. Sperl et al., REVERSIBLE HEPATIC VENOOCCLUSIVE DISEASE IN AN INFANT AFTER CONSUMPTION OF PYRROLIZIDINE-CONTAINING HERBAL TEA, European journal of pediatrics, 154(2), 1995, pp. 112-116

Authors: WENDEL U EISSLER A SPERL W SCHADEWALDT P
Citation: U. Wendel et al., ON THE DIFFERENCES BETWEEN URINARY METABOLITE EXCRETION AND ODD-NUMBERED FATTY-ACID PRODUCTION IN PROPIONIC AND METHYLMALONIC ACIDEMIAS, Journal of inherited metabolic disease, 18(5), 1995, pp. 584-591

Authors: SOLDER B PECHLANER C SPERL W SKLADAL D KUNZ F SHIN YS
Citation: B. Solder et al., FACTOR-XI AND PHOSPHORYLASE-B KINASE-DEFICIENCY, Journal of inherited metabolic disease, 18(1), 1995, pp. 89-90

Authors: DECSI T ZAKNUN D ZAKNUN J SPERL W KOLETZKO B
Citation: T. Decsi et al., LONG-CHAIN POLYUNSATURATES (LCP) IN MALNOURISHED CHILDREN WITH HUMAN IMMUNODEFICIENCY VIRUS-1 (HIV) INFECTION, Pediatric research, 38(3), 1995, pp. 431-431

Authors: DECSI T ZAKNUN D ZAKNUN J SPERL W KOLETZKO B
Citation: T. Decsi et al., LONG-CHAIN POLYUNSATURATED FATTY-ACIDS IN CHILDREN WITH SEVERE PROTEIN-ENERGY MALNUTRITION WITH AND WITHOUT HUMAN IMMUNODEFICIENCY VIRUS-1 INFECTION, The American journal of clinical nutrition, 62(6), 1995, pp. 1283-1288

Authors: LEHNERT W SPERL W SUORMALA T BAUMGARTNER ER
Citation: W. Lehnert et al., PROPIONIC ACIDEMIA - CLINICAL, BIOCHEMICAL AND THERAPEUTIC ASPECTS - EXPERIENCE IN 30 PATIENTS, European journal of pediatrics, 153(7), 1994, pp. 190000068-190000080

Authors: SPERL W SKLADAL D ENDRES W SPEER G GROKE K
Citation: W. Sperl et al., PARENTERAL ADMINISTRATION OF AMINO-ACIDS IN DISORDERS OF BRANCHED-CHAIN AMINO-ACID-METABOLISM, Journal of inherited metabolic disease, 17(6), 1994, pp. 753-754

Authors: SPERL W SKLADAL D LANZNASTER N SCHRANZHOFER R ZAUNSCHIRM G GNAIGER E PLOCHL E GELLERICH F
Citation: W. Sperl et al., POLAROGRAPHIC STUDIES OF SAPONIN-SKINNED MUSCLE-FIBERS IN PATIENTS WITH MITOCHONDRIAL MYOPATHIES, Journal of inherited metabolic disease, 17(3), 1994, pp. 307-310

Authors: SPERL W BART G VANIER MT CHRISTOMANOU H BALDISSERA I STEICHENGERSDORF E PASCHKE E
Citation: W. Sperl et al., A FAMILY WITH VISCERAL COURSE OF NIEMANN-PICK DISEASE, MACULAR HALO SYNDROME AND LOW SPHINGOMYELIN DEGRADATION RATE, Journal of inherited metabolic disease, 17(1), 1994, pp. 93-103
Risultati: 1-25 | 26-29