Literature DB >> 13214961

A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance.

J H MENKES, P L HURST, J M CRAIG.   

Abstract

Entities:  

Keywords:  BRAIN/diseases; HEREDITY; INFANT, NEWBORN/diseases; URINE

Mesh:

Year:  1954        PMID: 13214961

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


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  80 in total

1.  [MAPLE SYRUP DISEASE WITH FAMILIAL INCIDENCE].

Authors:  P B DIEZEL; K MARTIN
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1964-05-22

2.  [ON THE NOMENCLATURE OF CONGENITAL METABOLIC ANOMALIES].

Authors:  I SANO
Journal:  Klin Wochenschr       Date:  1964-02-01

Review 3.  INHERITED ENZYME DEFECTS: A REVIEW.

Authors:  T HARGREAVES
Journal:  J Clin Pathol       Date:  1963-07       Impact factor: 3.411

4.  MAPLE SYRUP URINE DISEASE.

Authors:  M A VOYCE; J N MONTGOMERY; G A LYNCH; J K BOWMAN
Journal:  Br Med J       Date:  1964-05-16

5.  DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).

Authors:  R G WESTALL
Journal:  Arch Dis Child       Date:  1963-10       Impact factor: 3.791

6.  DISORDERS OF AMINO-ACID TRANSPORT.

Authors:  M D MILNE
Journal:  Br Med J       Date:  1964-02-08

7.  [HETEROZYGOTE TEST FOR MAPLE SYRUP URINE DISEASE. DETERMINATION OF THE ENZYMATIC ACTIVITY OF ALPHA-KETOISOCAPROIC ACID OXIDASE IN LEUKOCYTES].

Authors:  H W GOEDDE; E RICHTER; C STAHLMANN; B SIXEL
Journal:  Klin Wochenschr       Date:  1963-10-01

8.  A survey of some hereditary metabolic diseases.

Authors:  R W WATTS
Journal:  Postgrad Med J       Date:  1960-08       Impact factor: 2.401

9.  Phenylketonuria: screening programs and testing methods.

Authors:  W R CENTERWALL; R F CHINNOCK; A PUSAVAT
Journal:  Am J Public Health Nations Health       Date:  1960-11

10.  Studies in maple syrup urine disease.

Authors:  C E DENT; R G WESTALL
Journal:  Arch Dis Child       Date:  1961-06       Impact factor: 3.791

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