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Your search keyword '"Makbule Haktan"' showing total 2 results
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2 results on '"Makbule Haktan"'

1. Screening for Inherited Metabolic Disorders: A New Look at Metabolic Screening Tests

Author

J. W. T. Seakins, B. C. Andrew, Makbule Haktan, and R. S. Ersser

Subjects
030213 general clinical medicine, 03 medical and health sciences, 0302 clinical medicine, Screening test, business.industry, Clinical Biochemistry, Medicine, 030209 endocrinology & metabolism, General Medicine, Urine, business, Bioinformatics
Abstract

Simple methods for the detection of inborn errors of metabolism which result in the accumulation of metabolites in blood or urine are described and the significance of abnormal findings reviewed.

Published
1972
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2. Progressive systemic scleroderma in an infant with partial phenylketonuria

Author

Beyhan Tüysüz, Ahmet Aydin, Hasan Yazici, H Bahat, S Altay, and Makbule Haktan

Subjects
Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Scleroderma, Systemic, integumentary system, business.industry, Phenylalanine, Infant, nutritional and metabolic diseases, Systemic scleroderma, medicine.disease, Dermatology, Scleroderma, nervous system diseases, Surgery, Pseudoscleroderma, Adrenal Cortex Hormones, Phenylketonurias, Genetics, Humans, Medicine, In patient, business, health care economics and organizations, Genetics (clinical)
Abstract

Pseudoscleroderma occurs occasionally in patients with phenylketonuria, but as far as we know scleroderma with visceral involvement has never been reported in phenylketonuria. Here we present a case of progressive systemic scleroderma with mild phenylketonuria

Published
1989
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