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Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome
(WILEY-BLACKWELL, 2011)
Wolcott-Rallison syndrome (WRS, OMIM 226980) is a rare autosomal recessive disorder characterized by permanent neonatal diabetes mellitus, epiphyseal dysplasia, and other multisystemic clinical manifestations. We described ...
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome
(Wiley-Blackwell, 2011-05-01)
Wolcott-Rallison syndrome (WRS, OMIM 226980) is a rare autosomal recessive disorder characterized by permanent neonatal diabetes mellitus, epiphyseal dysplasia, and other multisystemic clinical manifestations. We described ...
Displasia fibrosa craniofacial: relato de casoCraniofacial fibrous dysplasia: case report
(Centro de Ciências da Saúde da Universidade Federal do Espírito Santo (UFES), 2017)
Detection of hematopoietic maturation abnormalities by flow cytometry in myelodysplastic syndromes and its utility for the differential diagnosis with non-clonal disorders
(Pergamon-elsevier Science LtdOxfordInglaterra, 2007)
Morphological changes in the bone marrow of the dogs with visceral leishmaniasis
(Hindawi Publishing Corporation, 2014)
The aim of this study was to evaluate the most frequent lesions in the bone marrow of dogs naturally infected by Leishmania (Leishmania) chagasi. Thirty-three dogs sacrificed at the Zoonosis Control Center of Araçatuba, a ...
Maxillofacial Mazabraud’s syndrome: a case report & review
(Elsevier, 2018)
Mazabraud’s syndrome is characterized by myxomas of intramuscular type present in association with
fibrous dysplasia. Up to this day, approximately 80 cases of Mazabraud’s syndrome have been reported,
although in the ...
Maxillofacial Mazabraud's syndrome: A case report & review
(Elsevier Masson SAS, 2018)
Mazabraud’s syndrome is characterized by myxomas of intramuscular type present in association with
fibrous dysplasia. Up to this day, approximately 80 cases of Mazabraud’s syndrome have been reported,
although in the ...
FGF2 alters expression of the pyrophosphate/phosphate regulating proteins, PC-1, ANK and TNAP, in the calvarial osteoblastic cell line, MC3T3E1 (C4)
(Taylor & Francis LtdAbingdonInglaterra, 2005)