Familial Pancreatitis Associated with Hyperglycinuria

Author:

Bergström K.1,Hellström K.1,Kallner M.1,Lundh G.1

Affiliation:

1. Depts. of Clinical Chemistry and Internal Medicine, Serafimerlasarettet, and Department of Surgery, Södersjukhuset, Stockholm, Sweden

Publisher

Informa UK Limited

Subject

Gastroenterology

Reference19 articles.

1. Atfield, G. N. & Morris, C. i. 1961. Analytical separations by high-voltage paper electrophoresis amino acids in protein hydrolysates. Biochem. J. 81, 606–614.

2. Bergstrom, K., Gürtler, J. & Blomstrand, R. 1970. Trimethylsilylation of amino acids. I. Study of glycine and lysine TMS derivatives with gas-liquid chromatography-mass spectometry. Analyt. Biochem. 34, 74–87.

3. Trimethylsilylation of Amino Acids. II. Gas Chromatographic and Structural Studies on Trimethylsilyl Derivatives of Straight Chain Amino Acids.

4. Determination of Trypsin in Duodenal Fluid as a Test of Pancreatic Function

5. Burnett, C. H., Dent, C. E., Harper, C. & Warland, B. J. 1964. Vitamin D-resistant rickets. Analysis of twenty-four pedigrees with hereditary and sporadic cases. Amer. J. Med. 36, 222–232.

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1. Hyperglycinuria in a family with autosomal dominantly inherited cataract;Clinical Genetics;2008-04-23

2. HEREDITARY PANCREATITIS;Medical Clinics of North America;2000-05

3. HEREDITARY PANCREATITIS;Gastroenterology Clinics of North America;1994-12

4. Hereditary Disease of the Exocrine Pancreas;Clinics in Gastroenterology;1982-01

5. Genetic Aspects of Gastrointestinal Cancer;Clinics in Gastroenterology;1976-09

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