Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

173 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
[Socio-sanitary aspects and health of the preschool population].
García Caballero C, López Jiménez MR, Bonet de Luna C, Muñoz Calvo MT, Muñoz Hoyos A, López Rivas M, Aláez M, Cortizo E, Enrech Salazar S, Ferreiro A, et al. García Caballero C, et al. Among authors: ferreiro a. An Esp Pediatr. 1990 Dec;33(6):555-62. An Esp Pediatr. 1990. PMID: 2077999 Review. Spanish. No abstract available.
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome.
Villanova M, Mercuri E, Bertini E, Sabatelli P, Morandi L, Mora M, Sewry C, Brockington M, Brown SC, Ferreiro A, Maraldi NM, Toda T, Guicheney P, Merlini L, Muntoni F. Villanova M, et al. Among authors: ferreiro a. Neuromuscul Disord. 2000 Dec;10(8):541-7. doi: 10.1016/s0960-8966(00)00139-5. Neuromuscul Disord. 2000. PMID: 11053679
Macrophagic myofasciitis in childhood: a controversial entity.
Rivas E, Gómez-Arnáiz M, Ricoy JR, Mateos F, Simón R, García-Peñas JJ, Garcia-Silva MT, Martín E, Vázquez M, Ferreiro A, Cabello A. Rivas E, et al. Among authors: ferreiro a. Pediatr Neurol. 2005 Nov;33(5):350-6. doi: 10.1016/j.pediatrneurol.2005.05.024. Pediatr Neurol. 2005. PMID: 16243223
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.
Jungbluth H, Müller CR, Halliger-Keller B, Brockington M, Brown SC, Feng L, Chattopadhyay A, Mercuri E, Manzur AY, Ferreiro A, Laing NG, Davis MR, Roper HP, Dubowitz V, Bydder G, Sewry CA, Muntoni F. Jungbluth H, et al. Among authors: ferreiro a. Neurology. 2002 Jul 23;59(2):284-7. doi: 10.1212/wnl.59.2.284. Neurology. 2002. PMID: 12136074
173 results