187 related articles for article (PubMed ID: 4718759)
1. Serum carnosinase deficiency concomitant with mental retardation.
Murphey WH; Lindmark DG; Patchen LI; Housler ME; Harrod EK; Mosovich L
Pediatr Res; 1973 Jul; 7(7):601-6. PubMed ID: 4718759
[No Abstract] [Full Text] [Related]
2. Histopathology of the nervous system in carnosinase enzyme deficiency with mental retardation.
Terplan KL; Cares HL
Neurology; 1972 Jun; 22(6):644-55. PubMed ID: 4673339
[No Abstract] [Full Text] [Related]
3. Serum-carnosinase deficiency in carnosinaemia.
Perry TL; Hansen S; Love DL
Lancet; 1968 Jun; 1(7554):1229-30. PubMed ID: 4172777
[No Abstract] [Full Text] [Related]
4. A patient with a deficiency of serum-carnosinase activity.
van Heeswijk PJ; Trijbels JM; Schretlen ED; van Munster PJ; Monnens LA
Acta Paediatr Scand; 1969 Nov; 58(6):584-92. PubMed ID: 5378348
[No Abstract] [Full Text] [Related]
5. Serum carnosinase deficiency: a non-disabling phenotype?
Cohen M; Hartlage PL; Krawiecki N; Roesel RA; Carter AL; Hommes FA
J Ment Defic Res; 1985 Dec; 29 ( Pt 4)():383-9. PubMed ID: 4093964
[TBL] [Abstract][Full Text] [Related]
6. [Carnosinemia].
David M
Pediatrie; 1968; 23(1):117-9. PubMed ID: 4907174
[No Abstract] [Full Text] [Related]
7. Neurological disease in a child with carnosinase deficiency.
Wisniewski K; Fleisher L; Rassin D; Lassmann H
Neuropediatrics; 1981 May; 12(2):143-51. PubMed ID: 7266778
[TBL] [Abstract][Full Text] [Related]
8. A new sensitive method for the determination of serum carnosinase activity using l-carnosine-[I-14C] beta-alanyl as substrate.
van Munster PJ; Trijbels JM; van Heeswijk PJ; Moerkerk C; Schut-Jansen B
Clin Chim Acta; 1970 Aug; 29(2):243-8. PubMed ID: 5493180
[No Abstract] [Full Text] [Related]
9. Carnosinase and homocarnosinosis.
Lenney JF
J Oslo City Hosp; 1985; 35(2-3):27-40. PubMed ID: 3891936
[No Abstract] [Full Text] [Related]
10. Biochemical genetics of neurologic disease.
Rosenberg RN
N Engl J Med; 1981 Nov; 305(20):1181-93. PubMed ID: 6793870
[No Abstract] [Full Text] [Related]
11. [Causes of mental retardation in childhood (analysis of 414 cases)].
Hanefeld F; König E
Monatsschr Kinderheilkd (1902); 1974 Jul; 122(7):679-80. PubMed ID: 4471761
[No Abstract] [Full Text] [Related]
12. Prolidase deficiency and the biochemical assays used in its diagnosis.
Kurien BT; Patel NC; Porter AC; D'Souza A; Miller D; Matsumoto H; Wang H; Scofield RH
Anal Biochem; 2006 Feb; 349(2):165-75. PubMed ID: 16298326
[No Abstract] [Full Text] [Related]
13. Human cytosolic carnosinase: evidence of identity with prolinase, a non-specific dipeptidase.
Lenney JF
Biol Chem Hoppe Seyler; 1990 Feb; 371(2):167-71. PubMed ID: 2334521
[TBL] [Abstract][Full Text] [Related]
14. The genetic component in mentally retarded South Indian children.
Joshua GE
Indian J Med Res; 1974 Aug; 62(8):1251-60. PubMed ID: 4442985
[No Abstract] [Full Text] [Related]
15. Carnosinaemia.
Lancet; 1968 Apr; 1(7547):851-2. PubMed ID: 4171336
[No Abstract] [Full Text] [Related]
16. Carnosinase deficiency: a new variant with high residual activity.
Fleisher LD; Rassin DK; Wisniewski K; Salwen HR
Pediatr Res; 1980 Apr; 14(4 Pt 1):269-71. PubMed ID: 7375183
[TBL] [Abstract][Full Text] [Related]
17. Prolidase deficiency: an inborn error of metabolism with major dermatological manifestations.
Der Kaloustian VM; Freij BJ; Kurban AK
Dermatologica; 1982 May; 164(5):293-304. PubMed ID: 7095220
[No Abstract] [Full Text] [Related]
18. Actalasemia and hypocatalasemia in the Orient.
Takahara S
Semin Hematol; 1971 Oct; 8(4):397-416. PubMed ID: 5127632
[No Abstract] [Full Text] [Related]
19. Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease.
Konrad PN; McCarthy DJ; Mauer AM; Valentine WN; Paglia DE
J Pediatr; 1973 Mar; 82(3):456-60. PubMed ID: 4698932
[No Abstract] [Full Text] [Related]
20. Homocarnosinosis: hypercarnosinuria.
Lunde H; Sjaastad O; Gjessing L
J Neurochem; 1982 Jan; 38(1):242-5. PubMed ID: 7108529
[No Abstract] [Full Text] [Related]
[Next] [New Search]