C. Delgado-Pecellín

发表

Molecular epidemiology and genotype–phenotype correlation in phenylketonuria patients from South Spain

M. Couce, B. Pérez, L. Desviat, 2013, Journal of Human Genetics.

Newborn Screening for Primary T- and B-Cell Immune Deficiencies—A Prospective Study in Andalucía

J. Soto, O. Neth, P. Olbrich, 2017 .

[A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopenia].

R. Rodero, S. Borte, P. Ybot‐González, 2014, Anales de pediatria.

La PCR-as al mes de implantar un stent coronario metálico puede ser predictora de eventos adversos tardíos

A. Cayuela, C. Delgado-Pecellín, J. Fournier, 2008 .

[The high-sensitivity C-reactive protein level one month after bare-metal coronary stenting may predict late adverse events].

A. Cayuela, C. Delgado-Pecellín, J. Fournier, 2008, Revista espanola de cardiologia.

What are the biochemical parameters of pleural fluid that best identify parapneumonic effusions?

A. Leon-Justel, J. Guerrero, J. D. Santotoribio, 2009, Annals of clinical biochemistry.

Prospective neonatal screening for severe T‐ and B‐lymphocyte deficiencies in Seville

P. Soler-Palacín, S. Borte, O. Neth, 2016, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program

C. Pérez-Cerdá, B. Merinero, M. Ugarte, 2019, European Journal of Human Genetics.

Neonatal Screening for Sickle Cell Disease in Western Andalusia: Results and Lessons Learnt after 3 Years of Implementation

A. I. Álvarez-Ríos, C. Delgado-Pecellín, S. Payán-Pernía, 2022, American Journal of Perinatology.

Acrodermatitis Acidemica: Experience of 5 Years in Andalusia

J. Dominguez-Cruz, J. Conejo-Mir, J. Bernabéu-Wittel, 2010, Pediatric dermatology.

Evaluation of the Congenital Hypothyroidism Detection Strategy in Extremely Preterm Infants in Western Andalusia

C. Delgado-Pecellín, E. Melguizo-Madrid, R. Rubio-Sánchez, 2021, American Journal of Perinatology.

Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency

A. Ribes, E. Martins, L. Diogo, 2013, Orphanet Journal of Rare Diseases.

A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopaenia

R. Rodero, S. Borte, P. Ybot‐González, 2014 .

Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program

C. Pérez-Cerdá, B. Merinero, M. Ugarte, 2019, European Journal of Human Genetics.

[Results of the neonatal screening on Western Andalusia after a decade of experience.]

Enrique Melguizo Madrid, M. Bueno Delgado, C. Delgado-Pecellín, 2020, Revista espanola de salud publica.