Hipoplasia tímica en un niño con fibrosis quística

de la Guardia Peña, Odalis; Ustariz García, Catalino; García García, María de los Á; Morera Barrios, Luz M; Chang Monteagudo, Arturo; Lavaut Sánchez, Kalia.
Rev. cuba. hematol. inmunol. hemoter ; 30(1): 74-80, ene.-mar. 2014.
Artículo en Español | LILACS | ID: lil-705666

Documentos relacionados

  1. Thyroid hemiagenesis with compensatory hypertrophy of the remaining lobe: A case report.
  2. Two Cases of Congenital Hypothyroidism Revealing Thyroid Agenesis.
  3. Hipoplasia tímica en un niño con fibrosis quística
  4. NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis.
  5. Concurrence of Thyrolipomatosis with Hyperthyroidism and Ectopic Thyroid Tissue.
  6. Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
  7. GWAS of thyroid dysgenesis identifies a risk locus at 2q33.3 linked to regulation of Wnt signaling.
  8. The mutation screening in candidate genes related to thyroid dysgenesis by targeted next-generation sequencing panel in the Chinese congenital hypothyroidism.
  9. [Ectopic thyroid tissue after total thyroidectomy].
  10. Approach to the Patient With Congenital Hypothyroidism.