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2. [Hereditary tyrosinemia and vitamin-dependent rickets in Saguenay. A genetic and demographic approach]. Bouchard G; Laberge C; Scriver CR Union Med Can; 1985 Aug; 114(8):633-6. PubMed ID: 4060342 [No Abstract] [Full Text] [Related]
3. [Chromatographic studies of aminoaciduria in rickets]. Wolyńska-Bochner S Ann Acad Med Stetin; 1966; 12():489-507. PubMed ID: 5921239 [No Abstract] [Full Text] [Related]
4. [Changes in amino acid metabolism in several genetically determined diseases of the nervous system]. Badalian LO; Gusev EI; Koroleva IA Vestn Akad Med Nauk SSSR; 1969; 24(12):45-52. PubMed ID: 4248256 [No Abstract] [Full Text] [Related]
5. Ocular manifestations of familial hyperlysinemia. Smith TH; Holland MG; Woody NC Trans Am Acad Ophthalmol Otolaryngol; 1971; 75(2):355-60. PubMed ID: 5557172 [No Abstract] [Full Text] [Related]
6. Aminoaciduria in bone diseases in children. Opieńska-Blauth J; Gebala A; Sanecka-Obacz M; Kozlowska T; Stryjecka M Ann Paediatr; 1966; 207(2):115-24. PubMed ID: 5953604 [No Abstract] [Full Text] [Related]
9. [Disturbances in histidine metabolism in familial stuttering]. Galamon T; Szulc-Kuberska J; Tronczyńska J Pol Tyg Lek; 1968 Sep; 23(32):1208-10. PubMed ID: 5687194 [No Abstract] [Full Text] [Related]
10. [Vitamin-resistent rickets, occuring at school age, associated with specific hyperaminoaciduria]. Donath A; Käser H; Rossi E Schweiz Med Wochenschr; 1966 Apr; 96(13):416-24. PubMed ID: 5984004 [No Abstract] [Full Text] [Related]
11. [Reflections on some familial cases of late rickets of various origins observed in 3 siblings]. Marchal C; Charles JM Arch Fr Pediatr; 1967 Jan; 24(1):124-5. PubMed ID: 6031459 [No Abstract] [Full Text] [Related]
12. [Chorio-retinal degenerations and aminoaciduria. III. Atrophia gyrata]. Rodriguez Caballero ML Arch Ophtalmol Rev Gen Ophtalmol; 1975 Dec; 35(12):973-4. PubMed ID: 132162 [No Abstract] [Full Text] [Related]
13. [Problems of phenotypic similarity and differential diagnostic of hereditary diseases in children]. Barashnev IuI Vestn Akad Med Nauk SSSR; 1982; (6):47-51. PubMed ID: 7051616 [No Abstract] [Full Text] [Related]
14. [Hyperaminoaciduria]. Prader A Schweiz Med Wochenschr; 1966 Jan; 96(2):53-6. PubMed ID: 5985557 [No Abstract] [Full Text] [Related]
15. A study of aminoacidemia and aminoaciduria in epileptic children. Tudor I; Tănase-Mogoş I; Tănăsie E; Bădescu E; Răşcanu M Neurol Psychiatr (Bucur); 1976; 14(4):277-82. PubMed ID: 1024264 [No Abstract] [Full Text] [Related]
16. [Evaluation of aminoaciduria following surgery in children]. Pavesio D; Bardini T; Delfino U Minerva Pediatr; 1967 May; 19(21):1023-7. PubMed ID: 5609617 [No Abstract] [Full Text] [Related]
17. [Chronic hereditary tyrosinemia: a possible cause of rickets]. Napoli V; Bagnolesi P; Coppa GV; Ferri G Radiol Med; 1985 May; 71(5):348-51. PubMed ID: 4059603 [No Abstract] [Full Text] [Related]
18. Two cases of aminoaciduria, ocular changes and retarded mental and somatic development (Lowe's syndrome). TERSLEV E Acta Paediatr (Stockh); 1960 Sep; 49():635-44. PubMed ID: 13776045 [No Abstract] [Full Text] [Related]