146 related articles for article (PubMed ID: 14222346)
1. A SEX-LINKED DISORDER WITH MENTAL AND PHYSICAL RETARDATION CHARACTERIZED BY CEREBROCORTICAL ATROPHY AND INCREASE OF GLUTAMIC ACID IN THE CEREBROSPINAL FLUID.
YOSHIDA T; TADA K; MIZUNO T; WADA Y; AKABANE J; OGASAWARA J; MINAGAWA A; MORIKAWA T; OKAMURA T
Tohoku J Exp Med; 1964 Aug; 83():261-9. PubMed ID: 14222346
[No Abstract] [Full Text] [Related]
2. ABNORMAL AMINO-ACID EXCRETION IN CEREBRAL DISEASE.
GORDON N; WILSON VK
Dev Med Child Neurol; 1963 Dec; 5():586-92. PubMed ID: 14090617
[No Abstract] [Full Text] [Related]
3. MENTAL RETARDATION AND ABNORMAL AMINOACIDURIAS OCCURRING IN A FAMILY.
ANYON CP
N Z Med J; 1965 Jan; 64():3-7. PubMed ID: 14259628
[No Abstract] [Full Text] [Related]
4. EVALUATION OF THE AMINO ACID EXCRETION PATTERN OF MENTAL RETARDATES AS A SCREENING TECHNIQUE FOR INBORN ERRORS OF METABOLISM.
STAMBAUGH R; DAVIDSON DT
J Pediatr; 1964 Aug; 65():301-3. PubMed ID: 14198421
[No Abstract] [Full Text] [Related]
5. THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.
DIGEORGE AM; AUERBACH VH
Pediatr Clin North Am; 1963 Aug; 10():723-44. PubMed ID: 14145016
[No Abstract] [Full Text] [Related]
6. HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
CARSON NA; CUSWORTH DC; DENT CE; FIELD CM; NEILL DW; WESTALL RG
Arch Dis Child; 1963 Oct; 38(201):425-36. PubMed ID: 14065982
[No Abstract] [Full Text] [Related]
7. [TESTS FOR AMINO ACIDS IN URINE].
SANO I; KAKIMOTO T
No To Shinkei; 1964 Oct; 16():868-72. PubMed ID: 14220108
[No Abstract] [Full Text] [Related]
8. [QUANTITATIVE DEVIATIONS ON THE BORDERLINE OF THE NORM IN THE FREE AMINO ACIDS OF SERUM AND URINE IN MENTALLY DEFECTIVE CHILDREN].
HIRSCH W; MEX A; VOGEL F
Monatsschr Kinderheilkd (1902); 1963 Sep; 111():344-53. PubMed ID: 14089112
[No Abstract] [Full Text] [Related]
9. [ON A FAMILIAL DISEASE WITH AN UNUSUAL NEUROLOGIC SYMPTOM COMBINATION, OLIGOPHRENIA, DEMENTIA, MULTIPLE SKIN ULCERATIONS, SPLENOMEGALY AND AMINO ACID METABOLIC DISORDERS].
BRUCK J; GERSTENBRAND F; PROSENZ P; SANTLER R; SCHOBEL B; WEWALKA F
Dtsch Z Nervenheilkd; 1964 Feb; 185():579-97. PubMed ID: 14158292
[No Abstract] [Full Text] [Related]
10. IDIOPATHIC HYPERVALINEMIA: PROBABLY A NEW ENTITY OF INBORN ERROR OF VALINE METABOLISM.
WADA Y; TADA K; MINAGAWA A; YOSHIDA T; MORIKAWA T; OKAMURA T
Tohoku J Exp Med; 1963 Oct; 81():46-55. PubMed ID: 14077060
[No Abstract] [Full Text] [Related]
11. A MULTIVARIATE ANALYSIS OF AMINO-ACID EXCRETIONS.
DINGMAN HF; WRIGHT SW
J Ment Defic Res; 1964 Jun; 8():77-83. PubMed ID: 14171297
[No Abstract] [Full Text] [Related]
12. FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.
EFRON ML
N Engl J Med; 1965 Jun; 272():1243-54. PubMed ID: 14290545
[No Abstract] [Full Text] [Related]
13. DISTURBANCES OF COPPER AND AMINO ACID METABOLISM IN CLINICALLY HEALTHY RELATIVES OF PATIENTS WITH HEPATOLENTICULAR DEGENERATION.
PATRUNOVA VP
Fed Proc Transl Suppl; 1964; 23():340-2. PubMed ID: 14145670
[No Abstract] [Full Text] [Related]
14. INDOLYLACROYL GLYCINE EXCRETION IN A FAMILY WITH MENTAL RETARDATION.
MELLMAN WJ; BARNESS LA; TEDESCO TA; BESSELMAN D
Clin Chim Acta; 1963 Nov; 8():843-7. PubMed ID: 14089554
[No Abstract] [Full Text] [Related]
15. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.
EFRON ML; YOUNG D; MOSER HW; MACCREADY RA
N Engl J Med; 1964 Jun; 270():1378-83. PubMed ID: 14152868
[No Abstract] [Full Text] [Related]
16. HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES.
CARSON NA; DENT CE; FIELD CM; GAULL GE
J Pediatr; 1965 Mar; 66():565-83. PubMed ID: 14264314
[No Abstract] [Full Text] [Related]
17. HOMOCYSTINURIA.
KOMROWER GM; WILSON VK
Proc R Soc Med; 1963 Nov; 56(11):996-7. PubMed ID: 14084422
[No Abstract] [Full Text] [Related]
18. THE OCULO-CEREBRO-RENAL SYNDROME OF LOWE.
RICHARDS W; DONNELL GN; WILSON WA; STOWENS D; PERRY T
Am J Dis Child; 1965 Mar; 109():185-203. PubMed ID: 14246065
[No Abstract] [Full Text] [Related]
19. HYDROXYPROLINEMIA. II. A RARE METABOLIC DISEASE DUE TO A DEFICIENCY OF THE ENZYME "HYDROXYPROLINE OXIDASE".
EFRON ML; BIXBY EM; PRYLES CV
N Engl J Med; 1965 Jun; 272():1299-309. PubMed ID: 14299138
[No Abstract] [Full Text] [Related]
20. [CITRULLINURIA].
FREYCON F; FREYCON MT
Pediatrie; 1963; 18():847-9. PubMed ID: 14106631
[No Abstract] [Full Text] [Related]
[Next] [New Search]
