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Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review.
Genes (Basel). 2022 Dec 16;13(12):2377. doi: 10.3390/genes13122377.
Genes (Basel). 2022.
PMID: 36553645
Free PMC article.
Review.
Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.
Coeli FB, Ferraz LF, Lemos-Marini SH, Rigatto SZ, Belangero VM, de-Mello MP.
Coeli FB, et al.
Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1277-81. doi: 10.1590/s0004-27302008000800012.
Arq Bras Endocrinol Metabol. 2008.
PMID: 19169481
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Hypercalcemia in children: three cases report with unusual clinical presentations.
Garbim BB, D Ávila L, Rigatto SZP, Quadros KRDS, Belangero VMS, Oliveira RB.
Garbim BB, et al. Among authors: rigatto szp.
J Bras Nefrol. 2017 Apr-Jun;39(2):213-216. doi: 10.5935/0101-2800.20170036.
J Bras Nefrol. 2017.
PMID: 29069246
Free article.
English, Portuguese.
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Pain syndrome induced by calcineurin inhibitor and resolved by conversion to sirolimus in a child after kidney transplantation: a case report.
Prates LC, Rigatto SZ, Lutaif AC, Oliveira LC, Pereira LM, Passerotti LC, Belangero VM.
Prates LC, et al.
Transplant Proc. 2012 Oct;44(8):2510-1. doi: 10.1016/j.transproceed.2012.07.138.
Transplant Proc. 2012.
PMID: 23026634
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Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.
Macedo LC, Soardi FC, Ananias N, Belangero VM, Rigatto SZ, De-Mello MP, D'Souza-Li L.
Macedo LC, et al.
Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1244-51. doi: 10.1590/s0004-27302008000800007.
Arq Bras Endocrinol Metabol. 2008.
PMID: 19169476
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[Hypercalcemia and multiple osteolytic lesions in a child with disseminated paracoccidioidomycosis and pulmonary tuberculosis].
Tresoldi AT, Pereira RM, Castro LC, Rigatto SZ, Belangero VM.
Tresoldi AT, et al.
J Pediatr (Rio J). 2005 Jul-Aug;81(4):349-52.
J Pediatr (Rio J). 2005.
PMID: 16106322
Portuguese.
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