Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jean-Pierre Colombo"'
Autor:
Jochen Reiss, Ryszard Słomski, Ingrid Braulke, Jean-Pierre Colombo, Elisabeth Schröder, Claudia Behrend
Publikováno v:
Human Genetics. 89
A girl with ornithine transcarbamylase (OTC) deficiency was investigated for molecular and cytogenetic abnormalities that might explain this phenotype. Analysis with polymorphic DNA markers indicated that the patient did not inherit paternal alleles
Publikováno v:
Virchows Archiv A Pathological Anatomy and Histology. 393:321-331
Inborn defects of urea synthesis, leading to hyperammonemia, are complex inherited disorders, whose structural sequelae in different tissues and organs have not yet been studied in detail. Ultrastructural investigations have been performed on two cas
Publikováno v:
Endocrinology. 67:693-697
The hyperglycemic action of serotonin was investigated in 6 normal and 10 adrenalectomized dogs. In normal dogs, intravenous injections of serotonin were followed promptly by hyperglycemia, decreased liver glycogen and increased liver phosphorylase a
Autor:
Richard I Goldberg, Piero P. Foà, Jann W. Weber, Doris Kanameishi, Martin L Shulkind, Stanley Saperstein, Jean-Pierre Colombo
Publikováno v:
Diabetes. 10:122-129
Publikováno v:
Endocrinology. 67:248-251
The injection of deserpidine into the pancreato-duodenal artery of normal dogs is followed by a prompt rise in blood sugar concentration. This hypcrglycemia is not observed in previously depancreatized dogs. The results suggest that deserpidine cause
Publikováno v:
Analytical Chemistry. 33:151-153
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 172(2-3)
The determination of medium chain fatty acids in serum is a useful approach to the diagnosis of medium chain acyl-CoA dehydrogenase deficiency, an increasingly recognized cause of Reye-like syndrome in infants. A reliable and practical method requiri