Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vera M. S. Belangero"'
Autor:
Mara C. Moraes, Eduardo G. Roveri, Lívia C. Oliveira, Sumara Z. P. Rigatto, Vera M. S. Belangero, José Francisco C. Marques Jr
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 29, Iss 2, Pp 193-197 (2007)
A glomerulosclerose segmentar focal (GESF) é uma doença renal caracterizada por síndrome nefrótica, com freqüente progressão para insuficiência renal terminal. Nesta fase, o transplante renal, tanto com doador cadáver como intervivos, aparece
Externí odkaz:
https://doaj.org/article/d41957e8808a43d3886e1d7446f26239
Autor:
Antonia T. Tresoldi, Ricardo M. Pereira, Lelma C. Castro, Sumara Z. P. Rigatto, Vera M. S. Belangero
Publikováno v:
Jornal de Pediatria, Vol 81, Iss 4, Pp 349-352 (2005)
OBJETIVO: Descrever o caso de uma criança com paracoccidioidomicose, que apresentou hipercalcemia associada a múltiplas lesões osteolíticas. DESCRIÇÃO: Menino de 6 anos, internado com história de febre e hepatoesplenomegalia há 1 mês. À int
Externí odkaz:
https://doaj.org/article/2629c0527284410bbe5a06ad7be10163
WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome
Autor:
Mara S, Guaragna, Juliana G, Ribeiro de Andrade, Bárbara, de Freitas Carli, Vera M S, Belangero, Andréa T, Maciel-Guerra, Gil, Guerra-Júnior, Maricilda P, de Mello
Publikováno v:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 11(1)
Denys-Drash syndrome (DDS) is characterized by nephropathy, genital abnormalities, and predisposition to Wilms' tumor. DDS patients usually present heterozygous de novo germline WT1 mutations. The WT1 gene comprises 10 exons encoding the N-terminal t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70b7c6186f69a6b33fff3e0f4d4827d4
https://pubmed.ncbi.nlm.nih.gov/28081536
https://pubmed.ncbi.nlm.nih.gov/28081536
Autor:
Mara S, Guaragna, Thaís Lira, Cleto, Marcela Lopes, Souza, Anna Cristina G B, Lutaif, Luiz Cláudio Gonçalves, de Castro, Maria Goretti Moreira Guimarães, Penido, Andréa T, Maciel-Guerra, Vera M S, Belangero, Gil, Guerra-Junior, Maricilda P, De Mello
Publikováno v:
Nephrology (Carlton, Vic.). 21(9)
Autosomal recessive mutations in NPHS1 gene are a common cause of congenital nephrotic syndrome (CNS). The disorder is characterized by massive proteinuria that manifests in utero or in the neonatal period during the first 3 months of life. NPHS1 enc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f9a8e5c0d7fed3c9ebc443460ccad5c
https://pubmed.ncbi.nlm.nih.gov/26560236
https://pubmed.ncbi.nlm.nih.gov/26560236
Autor:
Antonia T, Tresoldi, Ricardo M, Pereira, Lelma C, Castro, Sumara Z P, Rigatto, Vera M S, Belangero
Publikováno v:
Jornal de pediatria. 81(4)
To describe the case of a child with paracoccidioidomycosis who presented hypercalcemia with multiple osteolytic lesions.A 6-year-old boy was admitted with a one-month history of fever and hepatosplenomegaly. On admission, he looked sick, pale, and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5da254fda0208a3169791a67b7aa4cf
https://pubmed.ncbi.nlm.nih.gov/16106322
https://pubmed.ncbi.nlm.nih.gov/16106322