Zobrazeno 1 - 10
of 36
pro vyhledávání: '"M. C. Carrascosa"'
Autor:
Maria M. C. Carrascosa, Tercio de Campos, Jéssica E. Sampaio, Rafaella R. F. Souza, Vitória L. Ribeiro, Maria L. N. Maia, Laura C. L. Gama, Mariana P. Severino, Nathan K. Semer, Otávio Rondon, Juliana B. M. Silva, Mariana Miyazi, Samara R. Domingues, Nathália E. S. Batalha, Delio E. Martins
Publikováno v:
Revista da Associação Médica Brasileira, Volume: 66, Issue: 6, Pages: 812-817, Published: 20 JUL 2020
Revista da Associação Médica Brasileira v.66 n.6 2020
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
Revista da Associação Médica Brasileira, Vol 66, Iss 6, Pp 812-817 (2020)
Revista da Associação Médica Brasileira v.66 n.6 2020
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB
Revista da Associação Médica Brasileira, Vol 66, Iss 6, Pp 812-817 (2020)
SUMMARY OBJECTIVE Assess the impact of COVID-19 on medical students’ internships in public and private institutions in Brasil, in addition to estimating the quality of the measures taken by their respective Universities in the face of the problem a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed7f29646920882da5be4b38bffce8a1
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302020000600812&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302020000600812&lng=en&tlng=en
Autor:
M. Bengoa Caamaño, J M Pardal-Fernandez, S. Álvarez, M C Carrascosa-Romero, C. de Cabo, M.C. Medina-Monzón
Publikováno v:
Neuromuscular Disorders. 28:881-884
Congenital myasthenic syndromes are a group of genetically determined rare diseases resulting from ultrastructural alterations in synaptic proteins. Up to 32 genes are known to be involved in those syndromes and many mutations have been reported, of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83c3cd92b125b1a458d7b30f02ec35ea
https://doi.org/10.1016/j.nmd.2018.06.020
https://doi.org/10.1016/j.nmd.2018.06.020
Akademický článek
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Autor:
C, Marcilla-Vazquez, A, Martinez-Gutierrez, M C, Carrascosa-Romero, M, Baquero-Cano, B, Alfaro-Ponce
Publikováno v:
Revista de neurologia. 67(12)
The different types of viral meningitis constitute a condition that is relatively frequent in newborn infants, although in many cases they are underdiagnosed due to the absence of pleocytosis in the cerebrospinal fluid (CSF).To describe the clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c46767d673abdb046d5a436c7ccc145
https://pubmed.ncbi.nlm.nih.gov/30536362
https://pubmed.ncbi.nlm.nih.gov/30536362
Publikováno v:
Neuropediatrics. 47:187-189
Antiepileptic drugs may occasionally increase seizure frequency or eliciting de novo seizure occurrence; the underlying mechanism of these effects is not known. The potential adverse effects of valproic acid in myoclonic astatic epilepsy have been no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe9ff07f90a3fbc69c3b5961dd6f827
https://doi.org/10.1055/s-0036-1579632
https://doi.org/10.1055/s-0036-1579632
Autor:
Javier Suela, Roque Tébar-Gil, Alberto Vidal-Company, María Luisa Martínez-Fernández, M C Carrascosa-Romero, Alexandra MacDonald, María Luisa Martínez-Frías, J M Pardal-Fernandez, Eva Bermejo-Sánchez
Publikováno v:
American Journal of Medical Genetics Part A. 161:2281-2290
We present a girl with the characteristic clinical picture associated with Marden-Walker syndrome (MWS; OMIM 248700), including mask-like face with blepharophimosis, joint contractures, intellectual disability, a multicystic dysplastic kidney and cer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4280dc341d7ba4e11e7dd7b053b720d
https://doi.org/10.1002/ajmg.a.35862
https://doi.org/10.1002/ajmg.a.35862
Autor:
J M, Pardal-Fernandez, M C, Carrascosa-Romero, A, Grande, M, Martinez-Gonzalez, B, Godes-Medrano
Publikováno v:
Revista de neurologia. 63(4)
Leucinosis is a severe neonatal metabolic disease. It is the consequence of the genetically determined enzyme deficiency of the complex formed by decarboxylase-dihydrolipoyl transacylase and dihydrolipoyl dehydrogenase, and of the subsequent accumula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a31420684fe0744f53db4d4a63c7e812
https://pubmed.ncbi.nlm.nih.gov/27439485
https://pubmed.ncbi.nlm.nih.gov/27439485
Publikováno v:
European Journal of Paediatric Neurology. 16:749-752
Pneumococcal meningoencephalitis (PME) is a life-threatening condition of the central nervous system (CNS), and is often the result of a complicated upper airway infection. Periodic Lateralized Epileptiform Discharges (PLEDs) are a typical electroenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a9812256ab67e6de90350e4e146e942
https://doi.org/10.1016/j.ejpn.2012.03.008
https://doi.org/10.1016/j.ejpn.2012.03.008