131 related articles for article (PubMed ID: 5624288)
21. [Inborn errors of metabolism and their occurrence].
Hanada M; Imamura T
Naika; 1966 Feb; 17(2):311-5. PubMed ID: 5960010
[No Abstract] [Full Text] [Related]
22. Hematological abnormalities in inborn errors of metabolism--how frequent are they? The Cretan experience.
Evangeliou A; Dafnis E; Perdikoyanni C; Spilioti M; Lionis C; Kalmanti M
Pediatr Hematol Oncol; 2002 Dec; 19(8):581-5. PubMed ID: 12487834
[TBL] [Abstract][Full Text] [Related]
23. Reversal of H2O2 toxicity in the acatalasemic mouse by catalase administration: Suggested model for possible replacement therapy of inborn errors of metabolism.
Feinstein RN; Braun JT; Howard JB
J Lab Clin Med; 1966 Dec; 68(6):952-7. PubMed ID: 5926191
[No Abstract] [Full Text] [Related]
24. [Primary hyperoxaluria: study of 4 cases].
Gonzalez Rodríguez L; Villarino Conde JA; Rodicio Díaz JL; Hernando Avendaño L
Rev Clin Esp; 1972 Apr; 125(1):27-36. PubMed ID: 5036746
[No Abstract] [Full Text] [Related]
25. Stop codon mutations in the flavin-containing monooxygenase 3 (FMO3) gene responsible for trimethylaminuria in a Japanese population.
Yamazaki H; Fujita H; Gunji T; Zhang J; Kamataki T; Cashman JR; Shimizu M
Mol Genet Metab; 2007 Jan; 90(1):58-63. PubMed ID: 16996766
[TBL] [Abstract][Full Text] [Related]
26. Cardiovascular manifestations of heritable disorders of connective tissue.
Pyeritz RE
Prog Med Genet; 1983; 5():191-302. PubMed ID: 6407064
[No Abstract] [Full Text] [Related]
27. [Oxalosis: two family studies in Tunisia (author's transl)].
Ramadhane MS; Khrouf N; Brauner R; Ben Jilani S; Hamza M; Hamza B
Ann Pediatr (Paris); 1982 Feb; 29(2):148-51. PubMed ID: 7059122
[No Abstract] [Full Text] [Related]
28. [Genetics in eye diseases].
Keith CG
Buch Augenarzt; 1981; (83):1-127. PubMed ID: 6784888
[No Abstract] [Full Text] [Related]
29. [Coexistence of ankylosing pelvispondylitis and cholinesterase deficiency in univitelline twins].
Karagevrekis C; Cellich M
Schweiz Rundsch Med Prax; 1973 Jul; 62(29):919-22. PubMed ID: 4720270
[No Abstract] [Full Text] [Related]
30. [Study of a family with goiter caused by an iodine organification defect].
Limbert E; Botelho L; Sobrinho L
Arq Patol; 1972 Aug; 44(2):139-46. PubMed ID: 4641690
[No Abstract] [Full Text] [Related]
31. The development of an inbred acatalasemic mouse. ANL-7535.
Camden RW; Flynn RJ; Feinstein RN
ANL Rep; 1968 Dec; ():189-90. PubMed ID: 5307179
[No Abstract] [Full Text] [Related]
32. [Hereditary acatalasemia in dogs].
Tanase H
Jikken Dobutsu; 1982 Oct; 31(4):323-5. PubMed ID: 7169091
[No Abstract] [Full Text] [Related]
33. [Frequency of atypical pseudocholinesterase in Greece].
Haidas S; Kattamis C; Liddell J
Pediatrie; 1971 Jun; 26(4):379-86. PubMed ID: 5568946
[No Abstract] [Full Text] [Related]
34. Acatalasia in two Peruvian siblings.
Delgado W; Calderón R
J Oral Pathol; 1979 Dec; 8(6):358-68. PubMed ID: 120431
[TBL] [Abstract][Full Text] [Related]
35. [Catalase deficiency in a case of cystic fibrosis].
Castelpietra L; Marchi AG; Mastella G
Minerva Pediatr; 1982 Sep; 34(17):705-7. PubMed ID: 7144712
[No Abstract] [Full Text] [Related]
36. Congenital creatine transporter deficiency.
deGrauw TJ; Salomons GS; Cecil KM; Chuck G; Newmeyer A; Schapiro MB; Jakobs C
Neuropediatrics; 2002 Oct; 33(5):232-8. PubMed ID: 12536364
[TBL] [Abstract][Full Text] [Related]
37. [Inherited urea cycle disorders in Finland].
Siitonen A; Salo MK
Duodecim; 2004; 120(1):61-70. PubMed ID: 14976809
[No Abstract] [Full Text] [Related]
38. Isolated growth hormone deficiency.
Wadia RS; Grant KB
J Assoc Physicians India; 1972 Feb; 20(2):183-6. PubMed ID: 5023637
[No Abstract] [Full Text] [Related]
39. [Three congenital metabolic diseases in the Faeroe Islands. Incidence, clinical and molecular genetic characteristics of Faeroese children with glycogen storage disease type IIIA, carnitine transporter deficiency and holocarboxylase synthetase deficiency].
Joensen F; Steuerwald EU; Rasmussen NH
Ugeskr Laeger; 2006 Feb; 168(7):667-70. PubMed ID: 16494802
[TBL] [Abstract][Full Text] [Related]
40. Microbodies in experimentally altered cells. V. Histochemical and cytochemical studies on the livers of rats and acatalasemic (Csb) mice treated with CPIB.
Reddy J; Bunyaratvej S; Svoboda D
Am J Pathol; 1969 Sep; 56(3):351-70. PubMed ID: 5822312
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]