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thallium and Inborn Errors of Metabolism

thallium has been researched along with Inborn Errors of Metabolism in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hassoun, A; Martin, JJ; Mercelis, R; Verstraeten, L	1
Rieger, H	1

Reviews

1 review(s) available for thallium and Inborn Errors of Metabolism

Article	Year
[Pathogenesis of various forms of arterial hypertension]. Journal of reproduction and fertility. Supplement, 1971, Volume: 14 Topics: Adrenal Gland Neoplasms; Adrenal Hyperplasia, Congenital; Aging; Aortic Coarctation; Aortic Valve Insufficiency; Arteriovenous Fistula; Autonomic Nervous System; Bionics; Contraceptives, Oral; Dysautonomia, Familial; Environmental Exposure; Glucocorticoids; Heart Block; Humans; Hyperaldosteronism; Hypertension; Hypertension, Renal; Metabolism, Inborn Errors; Neurons, Afferent; Neurons, Efferent; Pheochromocytoma; Pressoreceptors; Sodium; Sodium Chloride; Thallium; Thyroxine	1971

Article

Year

[Pathogenesis of various forms of arterial hypertension].

Journal of reproduction and fertility. Supplement, 1971, Volume: 14

Topics: Adrenal Gland Neoplasms; Adrenal Hyperplasia, Congenital; Aging; Aortic Coarctation; Aortic Valve Insufficiency; Arteriovenous Fistula; Autonomic Nervous System; Bionics; Contraceptives, Oral; Dysautonomia, Familial; Environmental Exposure; Glucocorticoids; Heart Block; Humans; Hyperaldosteronism; Hypertension; Hypertension, Renal; Metabolism, Inborn Errors; Neurons, Afferent; Neurons, Efferent; Pheochromocytoma; Pressoreceptors; Sodium; Sodium Chloride; Thallium; Thyroxine

1971

Other Studies

1 other study(ies) available for thallium and Inborn Errors of Metabolism

Article	Year
Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old man. Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 1989, Volume: 27, Issue:10 Topics: Aluminum; Blood Glucose; Cadmium; Creatinine; Erythrocyte Count; Humans; Lead; Male; Mercury; Metabolism, Inborn Errors; Middle Aged; Porphobilinogen Synthase; Porphyrins; Thallium	1989

Article

Year

Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old man.

Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 1989, Volume: 27, Issue:10

Topics: Aluminum; Blood Glucose; Cadmium; Creatinine; Erythrocyte Count; Humans; Lead; Male; Mercury; Metabolism, Inborn Errors; Middle Aged; Porphobilinogen Synthase; Porphyrins; Thallium

1989