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23 in total

1. PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

Authors: S TARUI; G OKUNO; Y IKURA; T TANAKA; M SUDA; M NISHIKAWA
Journal: Biochem Biophys Res Commun Date: 1965-05-03 Impact factor: 3.575

2. Erythrocyte enzyme deficiencies. Pyruvate kinase deficiency.

Authors: E C Gordon-Smith
Journal: J Clin Pathol Suppl (R Coll Pathol) Date: 1974

3. Red cell aldolase deficiency and hemolytic anemia: a new syndrome.

Authors: E Beutler; S Scott; A Bishop; N Margolis; F Matsumoto; W Kuhl
Journal: Trans Assoc Am Physicians Date: 1973

4. Fluorescent spot test for screening erythrocyte glucose-6-phosphate dehydrogenase deficiency in newborn babies.

Authors: C Y Yeung; H C Lai; W K Sin; N K Leung
Journal: J Pediatr Date: 1970-06 Impact factor: 4.406

5. Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome.

Authors: W N Valentine; H S Hsieh; D E Paglia; H M Anderson; M A Baughan; E R Jaffé; O M Garson
Journal: N Engl J Med Date: 1969-03-06 Impact factor: 91.245

6. Studies on erythrocyte metabolism in a case with hereditary deficiency of H-subunit of lactate dehydrogenase.

Authors: S Miwa; T Nishina; Y Kakehashi; M Kitamura; A Hiratsuka
Journal: Nihon Ketsueki Gakkai Zasshi Date: 1971-04

7. Hereditary hemolytic anemia with increased red cell adenosine deaminase (45- to 70-fold) and decreased adenosine triphosphate.

Authors: W N Valentine; D E Paglia; A P Tartaglia; F Gilsanz
Journal: Science Date: 1977-02-25 Impact factor: 47.728

Diagnosis of red blood cell enzymopathies in infants, children and adolescents.