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1987
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Enzyme
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ISSN 0013-9432
EISSN 2504-2564
Journal Name Change
Continued with Vol. 13 (1972) as: Enzyme.
Enzyme 1987, Vol. 38, No. 1-4
Special Lectures
The Cystic Fibrosis Locus
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Further Areas
Robert Williamson; Brandon Wainwright; Colin Cooper; Peter Scambler; Martin Farrall; Xavier Estivill; Peter Pedersen
Enzyme (1987) 38 (1-4): 8–13.
https://doi.org/10.1159/000469185
Title Page / Table of Contents
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Enzyme (1987) 38 (1-4): 1–6.
https://doi.org/10.1159/000469183
Presidential Lecture
Molecular Basis of Inborn Errors of Metabolism
Genetic Analysis of Human Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency
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Enzyme (1987) 38 (1-4): 36–44.
https://doi.org/10.1159/000469188
Molecular Biology of the Alpha-L-Fucosidase Gene and Fucosidosis
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Jon S. O'Brien; Patrick J. Willems; Hisao Fukushima; Jeffrey R. de Wet; John K. Darby; Richard Di Cioccio; Michael Fowler; Thomas B. Shows
Enzyme (1987) 38 (1-4): 45–53.
https://doi.org/10.1159/000469189
Fabry Disease:Molecular Diagnosis of Hemizygotes and Heterozygotes
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Enzyme (1987) 38 (1-4): 54–64.
https://doi.org/10.1159/000469190
Molecular Genetics of Familial Amyloidotic Polyneuropathy
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Kazunori Shimada; Shuichiro Maeda; Shoji Wakasugi; Tatsufumi Murakami; Shukuro Araki; Ken-ichi Yamamura
Enzyme (1987) 38 (1-4): 65–71.
https://doi.org/10.1159/000469191
Molecular Studies of Progressive Muscular Dystrophy(Duchenne)
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Enzyme (1987) 38 (1-4): 72–75.
https://doi.org/10.1159/000469192
Organic Acidemia
Recent Progress in Understanding Glutaric Acidemias
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Enzyme (1987) 38 (1-4): 76–79.
https://doi.org/10.1159/000469193
Hyperketotic States Due to Inherited Defects of Ketolysis
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J. M. Saudbray; N. Specola; B. Middleton; A. Lombes; J. P. Bonnefont; C. Jakobs; A. Vassault; C. Charpentier; R. Day
Enzyme (1987) 38 (1-4): 80–90.
https://doi.org/10.1159/000469194
Molecular Basis of Isovaleric Acidemia and Medium-Chain Acyl-CoA Dehydrogenase Deficiency
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Enzyme (1987) 38 (1-4): 91–107.
https://doi.org/10.1159/000469195
Congenital Lactic Acidosis
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Enzyme (1987) 38 (1-4): 108–114.
https://doi.org/10.1159/000469196
Chemical Diagnosis of Inherited Defects of Fatty Acid Metabolism and Ketogenesis
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Enzyme (1987) 38 (1-4): 115–123.
https://doi.org/10.1159/000469197
New Diagnostic Techniques for the Detection of Organic Acidemias
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Enzyme (1987) 38 (1-4): 124–131.
https://doi.org/10.1159/000469198
Novel Mechanism of Inborn Errors of Metabolism
Molecular Heterogeneity in Human ß-Galactosidase and Neuraminidase Deficiency
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H. Galjaard; R. willemsen; A. T. Hoogeveen; G. M. S. Mancini; S. Palmeri; F. W. Verheijen; A. D'Azzo
Enzyme (1987) 38 (1-4): 132–143.
https://doi.org/10.1159/000469199
Mutations Affecting Transport and Stability of Lysosomal Enzymes
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Enzyme (1987) 38 (1-4): 144–153.
https://doi.org/10.1159/000469200
Disorders of Lysosomal Membrane Transport -Cystinosis and Salla Disease
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Enzyme (1987) 38 (1-4): 154–160.
https://doi.org/10.1159/000469201
Genetic Diseases Caused by Peroxisomal Dysfunction
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R. B. H Schutzgens; R. J. A. Wanders; A. Nijenhuis; C. M. van den Hoek; H. S. A. Heymans; G. Schrakamp; E. M. Bleeker-Wagemakers; J. W. Delleman; A. W. Schram; J. M. Tager; H. van den Bosch
Enzyme (1987) 38 (1-4): 161–176.
https://doi.org/10.1159/000469202
Glycogen Storage Disease Type lb: Genetic Disorder Involving the Transport System of Intracellular Membrane
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Enzyme (1987) 38 (1-4): 177–183.
https://doi.org/10.1159/000469203
Impaired Insulin Binding and Excess Glucose Transport in Fibroblasts from a Patient with Leprechaunism
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Enzyme (1987) 38 (1-4): 184–193.
https://doi.org/10.1159/000469204
New Approach to the Treatment of Inborn Errors of Metabolism
Experience with Bone Marrow Transplantation for Inborn Errors of Metabolism
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Enzyme (1987) 38 (1-4): 194–206.
https://doi.org/10.1159/000469205
Molecular Basis of Phenylketonuria and Recombinant DNA Strategies for Its Therapy
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Enzyme (1987) 38 (1-4): 207–2013.
https://doi.org/10.1159/000469206
Urea Cycle Disorders
Molecular Aspects of Urea Cycle Enzymes and Related Disorders
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Enzyme (1987) 38 (1-4): 220–226.
https://doi.org/10.1159/000469208
Molecular Basis of Enzyme Abnormalities in Urea Cycle Disorders
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Takeyori Saheki; Keiko Kobayashi; Hitoshi Ichiki; Seiji Matuo; Mihciko Tatsuno; Yasushi Imamura; Ituro Inoue; Takashi Noda; Sumio Hagihara
Enzyme (1987) 38 (1-4): 227–232.
https://doi.org/10.1159/000469209
Diagnosis of Urea Cycle Disorders
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Enzyme (1987) 38 (1-4): 0223–241.
https://doi.org/10.1159/000469210
Hyperammonemia Related to Carnitine Metabolism with Particular Emphasis on Ornithine Transcarbamylase Deficiency
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Enzyme (1987) 38 (1-4): 251–255.
https://doi.org/10.1159/000469212
Lysosomal Diseases
Lysosomal Sialidase Deficiency: Increased Ganglioside Content in Autopsy Tissues of a Sialidosis Patient
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Enzyme (1987) 38 (1-4): 262–266.
https://doi.org/10.1159/000469214
Biochemical Heterogeneity in I-Cell Disease
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Shintaro Okada; Inui Koji; Masumi Furukawa; Mitsuo Midorikawa; Junji Nishimoto; Hyakuji Yabuuchi; Tomochika Kato; Mutsuko Watanabe; Shinsei Gasa; Akira Makita
Enzyme (1987) 38 (1-4): 267–272.
https://doi.org/10.1159/000469215
Pathochemistry, Pathogenesis and Enzyme Replacement in Multiple-Sulfatase Deficiency
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Enzyme (1987) 38 (1-4): 273–279.
https://doi.org/10.1159/000469216
α-Glucosidase Deficiency (Pompe’s Disease)
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J. M. Tager; R. P. J. Oude Elferink; A. Reuser; M. Kroos; L. A. Ginsel; J. A. M. Fransen; J. Klumperman
Enzyme (1987) 38 (1-4): 0280–285.
https://doi.org/10.1159/000469217
Phenylketonuria
Tetrahydrobiopterin Biosynthetic Pathway and Deficiency
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Enzyme (1987) 38 (1-4): 302–311.
https://doi.org/10.1159/000469220
Maternal Phenylketonuria
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Enzyme (1987) 38 (1-4): 312–320.
https://doi.org/10.1159/000469221
Treatment of Phenylketonuria with a Formula Consisting of Low-Phenylalanine Peptide
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Teruo Kitagawa; Misao Owada; Kikumaro Aoki; Shoichi Arai; Toshiaki Oura; Ichiro Matsuda; Yutaka Igarashi; Keiya Tada; Sumio Katayama; Wataru Hashida
Enzyme (1987) 38 (1-4): 321–327.
https://doi.org/10.1159/000469222
Author Index
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Enzyme (1987) 38 (1-4): 328.
https://doi.org/10.1159/000469223
Subject Index
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Enzyme (1987) 38 (1-4): 329–333.
https://doi.org/10.1159/000469224
