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Results: 1-8 |
Results: 8
THE THERAPEUTIC POTENTIAL OF ORAL CREATINE SUPPLEMENTATION IN MUSCLE DISEASE
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
HIGH-RESOLUTION RESPIROMETRY OF PERMEABILIZED SKELETAL-MUSCLE FIBERS IN THE DIAGNOSIS OF NEUROMUSCULAR DISORDERS
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
METABOLIC STROKE IN CARBAMYL-PHOSPHATE SYNTHETASE DEFICIENCY
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
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
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
CONGENITAL CATARACT AND FAMILIAL BRACHYDACTYLY IN CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME
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
FACTOR-XI AND PHOSPHORYLASE-B KINASE-DEFICIENCY
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
PARENTERAL ADMINISTRATION OF AMINO-ACIDS IN DISORDERS OF BRANCHED-CHAIN AMINO-ACID-METABOLISM
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
POLAROGRAPHIC STUDIES OF SAPONIN-SKINNED MUSCLE-FIBERS IN PATIENTS WITH MITOCHONDRIAL MYOPATHIES
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
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