Literature DB >> 19766262

[Usefulness of molecular analysis in the differential diagnosis of congenital 21-hidroxylase deficiency detected in neonatal screening].

Leandro Soriano Guillén, María Velázquez De Cuellar Paracchi, Begoña Ezquieta.   

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Year:  2009        PMID： 19766262     DOI： 10.1016/j.medcli.2009.06.008

Source DB:  PubMed          Journal:  Med Clin (Barc)        ISSN： 0025-7753            Impact factor:   1.725


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  2 in total

1.  Pseudohypoaldosteronism without nephropathy masking salt-wasting congenital adrenal hyperplasia genetically confirmed.

Authors:  Carla Balcells; Teresa Gili; Jacobo Pérez; Raquel Corripio
Journal:  BMJ Case Rep       Date:  2013-01-30

Review 2.  Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach.

Authors:  María Arriba; Begoña Ezquieta
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-29       Impact factor: 5.555
  2 in total

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