140 related articles for article (PubMed ID: 4135480)
1. [Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes].
Rochiccioli P; Dutau G
Arch Fr Pediatr; 1974 Jan; 31(1):25-36. PubMed ID: 4135480
[No Abstract] [Full Text] [Related]
2. [Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. I. 4 new cases].
Codaccioni JL; Pierron H; Rouault R; Bismuth J; Aquaron R
Ann Endocrinol (Paris); 1970; 31(6):1161-73. PubMed ID: 4101669
[No Abstract] [Full Text] [Related]
3. Biochemical and clinical studies in familial goitre caused by an iodotyrosine deiodinase defect.
Niall HD; Wellby ML; Hetzel BS; Hudson B; Chenoweth RA
Australas Ann Med; 1968 May; 17(2):89-95. PubMed ID: 4299848
[No Abstract] [Full Text] [Related]
4. Familial goiter due to an organification defect in euthyroid siblings.
Furth ED; Carvalho M; Vianna B
J Clin Endocrinol Metab; 1967 Aug; 27(8):1137-40. PubMed ID: 4166581
[No Abstract] [Full Text] [Related]
5. [Hypothyroidism due to congenital abnormality of thyroglobulin synthesis. Apropos of 3 cases].
Sultan C; Bismuth J; CASTAY M; Dumas R; Michel-Bechet M; Lissitzky S; Jean R
Arch Fr Pediatr; 1974 Jan; 31(1):11-23. PubMed ID: 4135555
[No Abstract] [Full Text] [Related]
6. [Congenital hypothyroisis with goiter caused by a genetic defect of thyroid hormone synthesis in 2 brothers].
Zhukovskiĭ MA; Sherbacheva LN
Pediatriia; 1970 Jul; 49(7):81-2. PubMed ID: 5479971
[No Abstract] [Full Text] [Related]
7. [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]
8. [Congenital absence of idothyronine deiodase].
Codaccioni JL; Vague J
Cesk Pediatr; 1968 Sep; 23(9):827-30. PubMed ID: 5685542
[No Abstract] [Full Text] [Related]
9. [Quantitative study of iodine metabolism in a case of hypothyroidism with goiter due to a defect of iodotyrosine deshalogenase].
Lissitzky S; Comar D; Rivière R; Codaccioni JL
Rev Fr Etud Clin Biol; 1965; 10(6):631-9. PubMed ID: 4158342
[No Abstract] [Full Text] [Related]
10. The influence of the plasma inorganic iodine concentration on thyroid function in dehalogenase deficiency.
Harden RM; Alexander WD; Papadopoulos S; Harrison MT; Macfarlane S
Acta Endocrinol (Copenh); 1967 Jun; 55(2):361-8. PubMed ID: 4165196
[No Abstract] [Full Text] [Related]
11. [Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
Kitlak W; Gebert P
Arch Kinderheilkd; 1968; 177(2):170-83. PubMed ID: 5723894
[No Abstract] [Full Text] [Related]
12. [Histopathologic aspects of goiter with disorders of hormonsynthesis. Apropos of 7 anatomoclinical cases].
Vilde F; Nezelof C
Ann Anat Pathol (Paris); 1966; 11(4):397-414. PubMed ID: 5972272
[No Abstract] [Full Text] [Related]
13. Clinical consequences of heterozygosity for autosomal-recessive diseases.
Vogel F
Clin Genet; 1984 May; 25(5):381-415. PubMed ID: 6373070
[TBL] [Abstract][Full Text] [Related]
14. Inborn errors of iodine metabolism in Greece.
Malamos B; Koutras DA; Sfontouris J; Rigopoulos G
Nucl Med (Stuttg); 1964 Apr; 4(1):45-55. PubMed ID: 5888657
[No Abstract] [Full Text] [Related]
15. [Diagnosis of iodotyrosine-dehalogenase deficiency after 3 normal pregnancies].
Elewaut A; Baele G; Schelstraete K; Vermeulen A
Ann Endocrinol (Paris); 1972; 33(6):599-605. PubMed ID: 4665419
[No Abstract] [Full Text] [Related]
16. [Late sporadic goiter in adults, with dehalogenase enzyme deficiency. Clinical, biochemical, isotope study].
Jaffiol C; Khalil R; Pastorello R; Baldet L; Mirouze J
Rev Fr Endocrinol Clin; 1969; 10(1):67-71. PubMed ID: 5802745
[No Abstract] [Full Text] [Related]
17. Genetic intrathyroidal hormone defects.
Ibrahim MS; Khalifa AS; Abdel-Wahab MF
J Egypt Med Assoc; 1970; 53(1):1-12. PubMed ID: 5507465
[No Abstract] [Full Text] [Related]
18. Congenital hypothyroidism. Aetiological and clinical aspects.
Mäenpää J
Arch Dis Child; 1972 Dec; 47(256):914-23. PubMed ID: 4119068
[TBL] [Abstract][Full Text] [Related]
19. [INBORN ERRORS IN THE SYNTHESIS OF THYROID HORMONES. REPORT ON 3 CASES].
ROOTWELT K; STEEN-JOHNSEN J
Tidsskr Nor Laegeforen; 1964 Oct; 84():1420-5. PubMed ID: 14226935
[No Abstract] [Full Text] [Related]
20. Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
Lizarralde G; Jones B; Seal US; Jones JE
J Clin Endocrinol Metab; 1966 Nov; 26(11):1227-31. PubMed ID: 4162599
[No Abstract] [Full Text] [Related]
[Next] [New Search]
