[MAPLE SYRUP DISEASE WITH FAMILIAL INCIDENCE]

Overview

Journal Virchows Arch Pathol Anat Physiol Klin Med

Specialties General Medicine
Pathology

Date 1964 May 22

PMID 14217031

Citations 7

Authors

P B DIEZEL

K Martin

Affiliations

Soon will be listed here.

Citing Articles

CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase.

Lisson G, Leupold D, BECHINGER D, Wallesch C Neuroradiology. 1981; 22(2):99-101.

PMID: 6170906 DOI: 10.1007/BF00344781.

[On the effect of dietetic prophylaxis on the myelogenesis of leucionsis (maple syrup urine disease)].

LINNEWEH F, SOLCHER H Klin Wochenschr. 1965; 43(17):926-30.

PMID: 5863558 DOI: 10.1007/BF01712059.

Spongy degeneration in the white matter of the central nervous system in the newborn: pathological findings in three infants, one with hyperglycinaemia.

Anderson J J Neurol Neurosurg Psychiatry. 1969; 32(4):328-37.

PMID: 4185340 PMC: 496522. DOI: 10.1136/jnnp.32.4.328.

[Evaluation of biochemical serum findings in mentally ill people].

Rabl R, Witt G, Mantzke I Acta Neuroveg (Wien). 1966; 29(1):95-110.

PMID: 4164179 DOI: 10.1007/BF01226710.

Ultrastructural findings in maple syrup urine disease in Poll Hereford calves.

Harper P, Healy P, Dennis J Acta Neuropathol. 1986; 71(3-4):316-20.

PMID: 3799144 DOI: 10.1007/BF00688055.

References

DENT C, WESTALL R . Studies in maple syrup urine disease. Arch Dis Child. 1961; 36:259-68. PMC: 2012780. DOI: 10.1136/adc.36.187.259. View

DANCIS J, Levitz M, WESTALL R . Maple syrup urine disease: branched-chain keto-aciduria. Pediatrics. 1960; 25:72-9. View

DANCIS J, Levitz M, Miller S, WESTALL R . Maple syrup urine disease. Br Med J. 1959; 1(5114):91-3. PMC: 1992207. DOI: 10.1136/bmj.1.5114.91. View

PATRICK A . Maple syrup urine disease. Arch Dis Child. 1961; 36:269-72. PMC: 2012762. DOI: 10.1136/adc.36.187.269. View

Ratzenhofer M, Lembeck F . [Model experiments on histochemical silver-reducing substrate]. Virchows Arch Pathol Anat Physiol Klin Med. 1959; 332(1):83-100. DOI: 10.1007/BF00968570. View

LANE M . Maple syrup urine disease. J Pediatr. 1961; 58:80-5. DOI: 10.1016/s0022-3476(61)80063-2. View

DANCIS J, HUTZLER J, Levitz M . Metabolism of the white blood cells in maple-syrup-urine disease. Biochim Biophys Acta. 1960; 43:342-3. DOI: 10.1016/0006-3002(60)90448-0. View

HOLT Jr L . [Maple syrup urine disease]. Monatsschr Kinderheilkd (1902). 1962; 110:165-6. View

NORTON P, ROITMAN E, Snyderman S, HOLT Jr L . A new finding in maple-syrup-urine disease. Lancet. 1962; 1(7219):26-7. DOI: 10.1016/s0140-6736(62)92646-6. View

10.

SILBERMAN J, DANCIS J, FEIGIN I . Neuropathological observations in maple syrup urine disease: branched-chain ketoaciduria. Arch Neurol. 1961; 5:351-63. DOI: 10.1001/archneur.1961.00450160001001. View

11.

MENKES J . Maple syrup disease; isolation and identification of organic acids in the urine. Pediatrics. 1959; 23(2):348-53. View

12.

MACKENZIE D, WOOLF L . Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency. Br Med J. 1959; 1(5114):90-1. PMC: 1992202. DOI: 10.1136/bmj.1.5114.90. View

13.

Wolman M . The spongy type of diffuse sclerosis. Brain. 1958; 81(2):243-7. DOI: 10.1093/brain/81.2.243. View

14.

Crome L, Dutton G, Ross C . Maple syrup urine disease. J Pathol Bacteriol. 1961; 81:379-84. DOI: 10.1002/path.1700810209. View

15.

MENKES J, HURST P, Craig J . A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. Pediatrics. 1954; 14(5):462-7. View

16.

SCHREIER K . [Maple syrup disease (Branched-chain decarboxylase deficiency)]. Dtsch Med Wochenschr. 1962; 87:2495-6. DOI: 10.1055/s-0028-1114120. View

17.

Meyer J . [Edematous disease of the central nervous system in early childhood]. Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1950; 185(1):35-51. DOI: 10.1007/BF00574919. View

18.

WESTALL R . DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA). Arch Dis Child. 1963; 38:485-91. PMC: 2019098. DOI: 10.1136/adc.38.201.485. View