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3. [Goiter and hypothyroidism due to a familial defect o deiodation of iodotyrosine]. Bigozzi U; Bigazzi M; Guazzelli R; Melani F Acta Genet Med Gemellol (Roma); 1967 Oct; 16(4):410-6. PubMed ID: 4173309 [No Abstract] [Full Text] [Related]
4. Studies of a sibship with apparent hereditary resistance to the intracellular action of thyroid hormone. Refetoff S; DeGroot LJ; Benard B; DeWind LT Metabolism; 1972 Aug; 21(8):723-56. PubMed ID: 5047916 [No Abstract] [Full Text] [Related]
5. [Familial oxalosis. Study of 2 cases. Attempted treatment]. Mathieu H; Gagnadoux MF; Mongour P; Czernichow P; Volter F; Kaplan M Bull Mem Soc Med Hop Paris; 1968; 119(9):719-30. PubMed ID: 5705150 [No Abstract] [Full Text] [Related]
6. [Biotinidase deficiency: importance of its neonatal diagnosis and early treatment]. Couce Pico ML; Martinón-Torres F; Castiñeiras DE; Alonso-Fernández JR; Fraga JM An Esp Pediatr; 1999 May; 50(5):504-6. PubMed ID: 10394193 [No Abstract] [Full Text] [Related]
7. [Medium chain Acyl-Coa Dehydrogenase deficiency. A diagnostic challenge for clinicians and laboratory]. Heinonen OJ; Iitiä A; Irjala K; Pulkki K Duodecim; 1996; 112(1):35-41. PubMed ID: 10590599 [No Abstract] [Full Text] [Related]
8. Clinical studies on iodine metabolism and thyroid function by I-131. II. Various indices of thyroid function in patients with thyroid disorders. KOSHIYAMA K Naika Hokan; 1962; 9():429-41. PubMed ID: 14034948 [No Abstract] [Full Text] [Related]
9. THE EFFECT OF METHYLTHIOURACIL ON THE METABOLISM OF 131-I-THYROXINE AND 127-I-THYROXINE. STOLC V Physiol Bohemoslov (1956); 1963; 12():365-71. PubMed ID: 14060625 [No Abstract] [Full Text] [Related]
10. [Clinical studies on iodine metabolism and thyroid function by I-131. I. Age difference of thyroid function in normal subjects]. KOSHIYANA K Naika Hokan; 1962; 9():381-92. PubMed ID: 14034950 [No Abstract] [Full Text] [Related]
11. [Familial deficiency on alpha-1-antitrypsin]. Wehinger H; Karitzky D; Witt I Z Kinderheilkd; 1971; 110(2):115-27. PubMed ID: 5580606 [No Abstract] [Full Text] [Related]
16. Inborn errors of metabolism in the molecular age. Valle DL; Mitchell GA Prog Med Genet; 1988; 7():100-29. PubMed ID: 3277250 [No Abstract] [Full Text] [Related]
17. [Hypothyroidism as a congenital metabolic disorder]. Blehová B; Höschl R Cesk Pediatr; 1968 Jul; 23(7):623-6. PubMed ID: 5681935 [No Abstract] [Full Text] [Related]
18. [Acatalasemia in Japan]. Takahara S Saishin Igaku; 1969 Jun; 24(6):1251-8. PubMed ID: 5805579 [No Abstract] [Full Text] [Related]
19. [DNA diagnosis of inborn errors of metabolism]. Ito M; Kuroda Y Nihon Rinsho; 1999 Dec; 57 Suppl():671-4. PubMed ID: 10778217 [No Abstract] [Full Text] [Related]