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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 13929692)

  • 1. Studies on a case of cretinism due to thyroidal dysgenesis.
    LEON N; WAJCHENBERG BL; PIERONI RR; de CINTRA A
    J Clin Endocrinol Metab; 1963 Jul; 23():615-9. PubMed ID: 13929692
    [No Abstract]   [Full Text] [Related]  

  • 2. [Thyroid insufficiency in children & accessory or aberrant thyroid tissue demonstrated by iodine-131].
    CERVINO JM; MORATO MANARO J; ZALDUA DE DELFINO E; MAGGIOLO J; NAVARRO A; SPREMOLLA F
    Rev Argent Endocrinol Metab; 1958 Sep; 4(3):254-73. PubMed ID: 13614739
    [No Abstract]   [Full Text] [Related]  

  • 3. The role of thyroid dysgenesis and maldescent in the etiology of sporadic cretinism.
    GABR M
    J Pediatr; 1962 Jun; 60():830-5. PubMed ID: 13896077
    [No Abstract]   [Full Text] [Related]  

  • 4. [Myxedema of the child; congenital myxedema due to hypothyroidism or thyroid agenesis and myxedema of cerebral origin in patients with brain diseases].
    CAMPO C; CARLI N; CHAPTAL J; JEAN R
    Arch Fr Pediatr; 1956; 13(5):509-36. PubMed ID: 13355481
    [No Abstract]   [Full Text] [Related]  

  • 5. [CONGENITAL HYPOTHYROIDISM AND THYROID ECTOPY DIAGNOSED WITH I-131].
    CHRZANOWSKA M; BUDZYNSKA A
    Endokrynol Pol; 1963; 14():409-14. PubMed ID: 14106222
    [No Abstract]   [Full Text] [Related]  

  • 6. Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.
    Kühnen P; Turan S; Fröhler S; Güran T; Abali S; Biebermann H; Bereket A; Grüters A; Chen W; Krude H
    J Clin Endocrinol Metab; 2014 Jan; 99(1):E169-76. PubMed ID: 24248179
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [CYTOLOGY OF THE ADENOHYPOPHYSIS IN A CASE OF THYROID AGENESIS].
    GARNEAU R; DEMERS PP; DESCHENES L; MAROIS M
    Laval Med; 1964 Sep; 35():766-70. PubMed ID: 14193272
    [No Abstract]   [Full Text] [Related]  

  • 8. [2 cases of minor myxedema with ectopic thyroid].
    VAGUE J; NICOLINO J; FAVIER G; MILLER G; DROGUE M; CALOTHY G
    Ann Endocrinol (Paris); 1963; 24():80-3. PubMed ID: 13995718
    [No Abstract]   [Full Text] [Related]  

  • 9. A subhyoid median ectopic thyroid.
    GRIEVE J
    Arch Dis Child; 1959 Feb; 34(173):18-9. PubMed ID: 13628224
    [No Abstract]   [Full Text] [Related]  

  • 10. Surgical management of subhyoid median ectopic thyroid.
    QUIGLEY WF; WILLIAMS LF; HUGHES CW
    Ann Surg; 1962 Feb; 155(2):305-8. PubMed ID: 14489488
    [No Abstract]   [Full Text] [Related]  

  • 11. [Demonstration of thyroid ectopia in congenital myxedema by iodine 131].
    NEIMANN N; KELLERSHOHN C; PIERSON M; MARTIN JY
    Rev Med Suisse Romande; 1960 Apr; 80():225-34. PubMed ID: 14426392
    [No Abstract]   [Full Text] [Related]  

  • 12. [ECTOPIC LINGUAL THYROID. CASE REPORTS AND CLINICO-THERAPEUTIC OBSERVATIONS].
    DELPRETE S; TOLLER G; SPINELLI-RESSI F
    Osp Maggiore; 1963 Jun; 58():579-90. PubMed ID: 14077465
    [No Abstract]   [Full Text] [Related]  

  • 13. [The iodine metabolism in the ectopic thyroid].
    DORTA T; BERAUD T; VANNOTTI A
    Schweiz Med Wochenschr; 1960 Feb; 90():150-3. PubMed ID: 13817724
    [No Abstract]   [Full Text] [Related]  

  • 14. [LINGUAL THYROID ECTOPY].
    ENGLARO GC; PICCOLI A; ZECCHIN R
    Minerva Otorinolaringol; 1963 Oct; 13():295-302. PubMed ID: 14115127
    [No Abstract]   [Full Text] [Related]  

  • 15. SURGICAL MANAGEMENT OF ECTOPIC THYROID: REPORT OF A CASE WITH SIMULTANEOUS LINGUAL AND SUBHYOID MEDIAN ECTOPIC THYROID.
    LONG RT; EVANS AM; BEGGS JH
    Ann Surg; 1964 Nov; 160(5):824-7. PubMed ID: 14236601
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetics of normal and abnormal thyroid development in humans.
    Szinnai G
    Best Pract Res Clin Endocrinol Metab; 2014 Mar; 28(2):133-50. PubMed ID: 24629857
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two puzzling cases of thyroid dysgenesis.
    Kuehnen P; Grueters A; Krude H
    Horm Res; 2009 Jan; 71 Suppl 1():93-7. PubMed ID: 19153515
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital hypothyroidism: from paracelsus to molecular diagnosis.
    Djemli A; Van Vliet G; Delvin EE
    Clin Biochem; 2006 May; 39(5):511-8. PubMed ID: 16730255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism.
    Khatami M; Heidari MM; Tabesh F; Ordooei M; Salehifar Z
    J Pediatr Endocrinol Metab; 2017 Aug; 30(8):857-862. PubMed ID: 28749785
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CONGENITAL AND JUVENILE HYPOTHYROIDISM DUE TO THYROID DYSGENESIS.
    MEDEIROS-NETO GA; DE ASSIS LM; NICOLAU W; COELHO-NETO AS; BLOISE W; LUTHOLD W; MONTENEGRO JL; PIERONI RR
    J Nucl Med; 1965 Apr; 6():275-86. PubMed ID: 14291078
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.