[Clinical and biochemical studies in pyridoxine-dependent seizures].
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Humans↗
Biomedical subjects
D Feist
Publications and source records attributed to D Feist.
[Indications and results of liver needle biopsy in childhood].
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Biopsy, Needle↗
[Maple syrup urine disease with an intermittent relatively benign course].
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Adult↗
[Hereditary fructose intolerance (author's transl)].
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Biopsy↗
[Studies of tryptophan metabolism in pyridoxin-dependent convulsions].
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Child, Preschool↗
[Therapy of cystinosis using a synthetic diet].
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Biopsy↗
[Ornithinemia, a newly recognized amino acid metabolism disorder with brain damage].
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Amino Acid Metabolism, Inborn Errors↗
Ornithinaemia. Another disorder of aminoacid metabolism associated with brain damage.
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Amino Acid Metabolism, Inborn Errors↗
[Ornithinemia, additional disorder of amino acid metabolism with brain damage].
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Amino Acids↗
[On the therapy of sepsis lenta in children].
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Adolescent↗
[D-penicillamine-induced IgA deficiency in the therapy of Wilson's disease].
Serum IgA deficiency was first noted in a 10 year old boy 8 months after the onset of D-penicillamine therapy. Special immunological examinations revealed a deficiency of the secretory component of IgA while cellular functions of T- and B-lymphocytes were normal. The patient showed discrete clinical signs compatible with IgA deficiency. Regular control of patients with Morbus Wilson and D-penicillamine treatment should include measurement of serum immunoglobulin levels.
Agammaglobulinemia↗
[Sonographic and computerized tomography study of congenital choledochal cyst].
In the neonatal period ultrasound and hepatobiliary functional scintigraphy are used to diagnose choledochal cysts. Initial sonography demonstrates hepatobiliary anatomy, hepatobiliary function is assessed by subsequent scintigraphy. The diagnosis can be confirmed by additional computed tomography as shown in this case report.
Common Bile Duct↗