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Congenital enzyme deficiency in carbohydrate metabolism. its significance for clinical pediatrics and human biochemical genetics

Schaub, J.; Osang, M.

Münchener Medizinische Wochenschrift 118(19): 609-614

1976

ISSN/ISBN: 0341-3098
PMID: 180406
Document Number: 107777
A review of the enzyme deficiencies of carbohydrate metabolism known at the present time is given. Through prominent clinical symptoms and consideration of food as a pathological agent, it is possible to suspect the various diseases before the results of the biochemical determinations are available. On account of the sometimes striking course, therapy can consequently be started at the earliest possible moment.

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Bakhtadze, G.G.; Anasashvili, A.T. 1976: Clinical significance of disorders of metabolism of carbohydrate-protein compounds in diffuse kidney diseases Terapevticheskii Arkhiv 48(7): 23-29
Vel'tishchev, I.E.; Badalian, L.O.; Tabolin, V.A. 1970: Achievements of modern medical genetics and their significance for pediatrics Pediatriia 49(12): 3-8
Bührdel, P.; Böhme, H.J. 1982: Use of leukocytes for enzyme tests in the diagnosis of carbohydrate metabolism disorders Kinderarztliche Praxis 50(6): 303-306
Gorbach, Z.V.; Maglysh, S.S.; Kubyshin, V.L.; Ostrovskiĭ, I.M. 1985: Characteristics of carbohydrate metabolism in the rat liver in thiamine deficiency Biokhimiia 50(8): 1261-1268
Ishida, Y.; Kawada, T.; Sugino, N. 1983: Urinary enzyme determination and its clinical significance. C. Enzyme derived from the kidney tubular epithelium--N-acetyl-beta-D-glucosaminidase. 11. Clinical significance of urinary NAG activity in patients with kidney diseases and those with kidney homografts Rinsho Byori. Japanese Journal of Clinical Pathology Spec no 56: 160-167
Goldstein, R.E.; Cherrington, A.D.; Reed, G.W.; Lacy, D.B.; Wasserman, D.H.; Abumrad, N.N. 1994: Effects of chronic hypercortisolemia on carbohydrate metabolism during insulin deficiency American Journal of Physiology 266(4 Pt 1): E618-E627
Beyreiss, K. 1972: Significance of congenital or acquired disorders of carbohydrate absorption for pediatries Deutsche Zeitschrift für Verdauungs- und Stoffwechselkrankheiten 32(1): 177-183
Chmiel, J.; Rybczyńska, M.; Pretczak, J.; Zawodna, K.; Lańczak, M. 1980: Study of main components of carbohydrate and enzyme metabolism in the blood of children with flaccid and spastic paralysis Chirurgia Narzadow Ruchu i Ortopedia Polska 45(2): 173-178
Cramp, D.G. 1970: Automated fluorimetric techniques based on NAD- and NADP-linked enzyme systems in the study of intermediary carbohydrate metabolism Journal of Medical Laboratory Technology 27(3): 359-382
Meyer, W.; Saglam, M.; Tanyolac, A.; Schwarz, R.; Hetzel, U. 1997: Histochemical and biochemical studies of the circannual aspects of carbohydrate-dependent energy metabolism of the hair follicles of Turkish Angora goats Schweizer Archiv für Tierheilkunde 139(2): 78-83
Botvin'ev, O.K.; Kurbatova, O.L.; Altukhov, I.P. 1980: Population genetics approach to the problem of nonspecific biological resistance of the human body. II. Clinical characteristics, congenital anomalies and genetic structure of sick children with attention to birth weight and length Genetika 16(10): 1884-1894
Yoshida, A. 1980: Biochemical genetics of human blood group (ABO) expression Seikagaku. Journal of Japanese Biochemical Society 52(4): 211-220
Harris, H. 1973: Potentialities of lymphocytoid lines in human biochemical genetics Birth Defects Original Article Series 9(1): 132-137
Masopust, J. 1980: Indications and interpretation of clinical-biochemical examinations in pediatrics. 2 Ceskoslovenska Pediatrie 35(7): 367-378
Lesnichnii, A.V. 1970: Effect of therapeutic physical exercise on the status of carbohydrate metabolism and certain indices of enzyme activity of blood serum in patients with diabetes mellitus Voprosy Kurortologii Fizioterapii i Lechebnoi Fizicheskoi Kultury 35(2): 151-153
Oseid, S.; Pruett, E.D. 1976: Studies in congenital generalized lipodystrophy. IV. Effect of muscular exercise on carbohydrate and fat metabolism including plasma levels of IRi and HGH Acta Endocrinologica 83(4): 839-855
Wu, L.Z.; Zeng, L.H.; Ma, Q.Y.; Xie, Y.J.; Chen, Y.Z.; Wu, D.Z. 1988: Hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness Japanese Journal of Ophthalmology 32(2): 236-245
Agboola-Abu, C.F.; Aligwekwe, P.K.; Olowu, A.O.; Kuku, S.F. 1999: Congenital adrenal hyperplasia due to 11-hydroxylase enzyme deficiency in three siblings. A brief report West African Journal of Medicine 18(2): 80-86
Stolecke, H. 1988: Significance of endocrinology in clinical pediatrics Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 136(2): 58-62
Gormsen, J.; Clausen, N.T. 1976: Inborn metabolism errors LV. Congenital "hypoprothrombinemia": Deficiency of II, VIi or X Ugeskrift for Laeger 138(24): 1462-1465