These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
99 related items for PubMed ID: 958671
1. Type I hyperprolinemia in a family suffering from aniridia and severe dystrophia of ocular tissues. Fusco G, Carlomagno S, Romano A, Rinaldi E, Cedrola G, Cianciaruso L, Curto A, Rosolia S, Auricchio G. Ophthalmologica; 1976; 173(1):1-10. PubMed ID: 958671 [No Abstract] [Full Text] [Related]
2. [Familial hyperprolinemia--a case in a family]. Oknińska A, Grygalewicz J, Kowalewska-Kantecka B, Iwańska J. Pol Arch Med Wewn; 1974 Feb; 51(2):189-97. PubMed ID: 4816363 [No Abstract] [Full Text] [Related]
3. Dietary treatment in hyperprolinaemia type II. Similä S. Acta Paediatr Scand; 1974 Mar; 63(2):249-56. PubMed ID: 4820590 [No Abstract] [Full Text] [Related]
4. [Type I hyperprolinemia. Study of a familial case]. Fontaine G, Farriaux JP, Dautrevaux M. Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477 [No Abstract] [Full Text] [Related]
5. [Familial hyperprolinemia with nephropathy]. Ortuño Mirete J, Guardiola Vicente JM, Botella García J. Rev Clin Esp; 1970 Jul 31; 118(2):141-50. PubMed ID: 5486371 [No Abstract] [Full Text] [Related]
6. Familial hyperprolinemia and mental retardation. A second metabolic type. Selkoe DJ. Neurology; 1969 May 31; 19(5):494-502. PubMed ID: 5815222 [No Abstract] [Full Text] [Related]
10. Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation. Di Rosa G, Pustorino G, Spano M, Campion D, Calabrò M, Aguennouz M, Caccamo D, Legallic S, Sgro DL, Bonsignore M, Tortorella G. Psychiatr Genet; 2008 Feb 31; 18(1):40-2. PubMed ID: 18197084 [Abstract] [Full Text] [Related]
11. Hyperprolinaemia in two successive generations of a North American Indian family. Perry TL, Hardwick DF, Lowry RB, Hansen S. Ann Hum Genet; 1968 May 31; 31(4):401-7. PubMed ID: 4299764 [No Abstract] [Full Text] [Related]
12. [Hyperprolinemia type II]. Thomsen B, Vetner M, Rosleff F, Reske-Nielsen E. Ugeskr Laeger; 1974 Nov 04; 136(45):2530. PubMed ID: 4420281 [No Abstract] [Full Text] [Related]
15. Hyperprolinemia and prolinuria in a new inbred strain of mice, PRO-Re. Blake RL, Russell ES. Science; 1972 May 19; 176(4036):809-11. PubMed ID: 5031477 [Abstract] [Full Text] [Related]
16. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family. Mollica F, Pavone L, Antener I. Pediatrics; 1971 Aug 19; 48(2):225-31. PubMed ID: 5560617 [No Abstract] [Full Text] [Related]
17. Hyperprolinaemia type II. Similä S. Fla Dent J; 1970 Aug 19; 2(2):143-50. PubMed ID: 5271041 [No Abstract] [Full Text] [Related]
20. A hypothesis on the homocystinuric's response to pyridoxine. Kelly S, Copeland W. Metabolism; 1968 Sep 19; 17(9):794-5. PubMed ID: 5674125 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]