BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 4135480)

  • 21. [On 3 cases of familial goiter due to probable congenital defect of hormonogenesis].
    Torino G; Esposito V
    Pediatria (Napoli); 1972; 80(4):388-97. PubMed ID: 4646632
    [No Abstract]   [Full Text] [Related]  

  • 22. The test of overloading L-diiodotyrosine (DIT) in the screening of iodotyrosine dehalogenase deficiency.
    Codaccioni JL; Rinaldi JP; Bismuth J
    Acta Endocrinol (Copenh); 1978 Jan; 87(1):95-105. PubMed ID: 579538
    [No Abstract]   [Full Text] [Related]  

  • 23. [Congenital hypothyroidism due to a type I hormonogenesis disorder. (3 cases in the same family and literature review)].
    Marie J; Rivière R; Hennequet A; Desbois JC; Seince JM
    Ann Pediatr (Paris); 1969; 16(6):424-36. PubMed ID: 4184994
    [No Abstract]   [Full Text] [Related]  

  • 24. [Thyroid peroxidase insufficiency as factor in the etiopathogenesis of endemic and sporadic goiter].
    Pentschew I; Papasow G; Warbanow W; Stantschewau M; Staykow T
    Endokrinologie; 1971 Apr; 57(3):353-7. PubMed ID: 4325994
    [No Abstract]   [Full Text] [Related]  

  • 25. [Familial cretinism with goiter--an inborn metabolic error].
    Blehová B
    Cesk Pediatr; 1968 Feb; 23(2):134-7. PubMed ID: 5663031
    [No Abstract]   [Full Text] [Related]  

  • 26. Radioisotopes in the diagnosis of hypothyroid states, iodine deficiency, and thyroiditis.
    Stanbury JB
    Nucl Med (Stuttg); 1965; ():Suppl 2:281+. PubMed ID: 4173570
    [No Abstract]   [Full Text] [Related]  

  • 27. Intrathyroidal defects in thyroid hormone synthesis. Use of radionuclides in diagnosis.
    Hofeldt FD; Dobbins WT; Block MB; Lufkin EG; Verdon TA
    Rocky Mt Med J; 1974 Oct; 71(10):570-5. PubMed ID: 4417978
    [No Abstract]   [Full Text] [Related]  

  • 28. Would I-123 di-iodotyrosine provide a harmless deiodination test? Concise communication.
    Aurengo A; Savoie F; Leger AF; Savoie JC
    J Nucl Med; 1983 Dec; 24(12):1143-8. PubMed ID: 6315903
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Pendred's syndrome: a clinical and biochemical study of abnormal thyroid hormone synthesis associated with congenital deaf-mutism].
    de Medeiros-Netto GA; Nicolau W; Cintra AB
    Rev Paul Med; 1969 Feb; 74(2):53-74. PubMed ID: 4190511
    [No Abstract]   [Full Text] [Related]  

  • 30. Thyroid disorders in children from birth to adolescence.
    Bettendorf M
    Eur J Nucl Med Mol Imaging; 2002 Aug; 29 Suppl 2():S439-46. PubMed ID: 12192543
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. II. Results of iodine treatment in 5 cases (8 years of recession in 1 case].
    Codaccioni JL; Pierron H; Rouault F; Aquaron R; Jaquet P
    Ann Endocrinol (Paris); 1970; 31(6):1174-82. PubMed ID: 4994830
    [No Abstract]   [Full Text] [Related]  

  • 32. [Methods and results of the thyroid gland function diagnosis in a Bavaria district with iodine defficiency].
    Heinze HG; Frey KW; Scriba PC
    Fortschr Geb Rontgenstr Nuklearmed; 1968 May; 108(5):596-606. PubMed ID: 4177075
    [No Abstract]   [Full Text] [Related]  

  • 33. [A study of 2 congenital hypothyroid goiters in siblings: identification of a genetic abnormality in thyroid hormonogenesis marked by the absence of thyroglobulin and by the iodination of unsuitable proteins rich in iodohistidine and deficient in thyroxine].
    Savoie JC; Massin JP; Sizonenko PC; Job JC
    Ann Endocrinol (Paris); 1973; 34(5):539-48. PubMed ID: 4136284
    [No Abstract]   [Full Text] [Related]  

  • 34. Thiourea-35S in the detection of iodine deficiency in the thyroid.
    Abdel-Wahab MF; Ibrahim MS; Megahed YM
    Endokrinologie; 1966 Dec; 50(5):280-6. PubMed ID: 5989930
    [No Abstract]   [Full Text] [Related]  

  • 35. [Functional and biochemical studies of subjects with goiter in a sub-endemic area].
    Bigazzi M; Guazzelli R; Farnararo M; Burci P; Melani F
    Riv Crit Clin Med; 1968; 68():Suppl 6:898+. PubMed ID: 5747763
    [No Abstract]   [Full Text] [Related]  

  • 36. Familial agoitrous cretinism accompanied by musclar hypertrophy.
    Cross HE; Hollander CS; Rimoin DL; McKusick VA
    Pediatrics; 1968 Feb; 41(2):413-20. PubMed ID: 5637792
    [No Abstract]   [Full Text] [Related]  

  • 37. [Hypothyroidism in gonadal dysgenesis].
    Ionescu A; Pencea V; Baran T; Floareş G; Petrescu O; Săvescu L; Mărgineanu L
    Stud Cercet Endocrinol; 1971; 22(4):287-301. PubMed ID: 4109601
    [No Abstract]   [Full Text] [Related]  

  • 38. Iodine kinetics in organification defect.
    Negri M; De Luca F; Cramarossa L; Benedetti GA
    Folia Endocrinol; 1967 Apr; 20(2):205-13. PubMed ID: 4169478
    [No Abstract]   [Full Text] [Related]  

  • 39. Inborn errors of thyroid hormone biosynthesis.
    de Vijlder JJ; Ris-Stalpers C; Vulsma T
    Exp Clin Endocrinol Diabetes; 1997; 105 Suppl 4():32-7. PubMed ID: 9439912
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Endemic goiter in Tyrol. II. Studies on iodine kinetics in goiter and normal thyroid glands].
    Riccabona G
    Acta Endocrinol (Copenh); 1968 Feb; 57(2):296-306. PubMed ID: 4169736
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.