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Regina Matsunaga Martin

Showing results (1-10 of 21) with videos related to

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Arquivos Brasileiros De Endocrinologia E Metabologia|May 21, 2010
Bone quality and osteoporosis therapyRegina Matsunaga Martin, Pedro Henrique S Correa
Bone|February 9, 2016
Failure of tooth eruption and brachydactyly in pseudohypoparathyroidism are not related to plasma parathyroid hormone-related protein levelsMariana Tenorio Antunes Reis, Diogo Toledo Matias, Maria Estela Justamante de Faria, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levelsMariana Tenorio Antunes Reis, Andreina Cattani, Berenice Bilharinho Mendonca, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|July 20, 2025
Brown tumor of hyperparathyroidism in the maxillofacial region: a retrospective study with 19 patientsBeatriz Afonso Chiliti, Regina Matsunaga Martin, Alan Roger Santos-Silva, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|April 7, 2011
New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT)Luiza Souza Rodrigues, Ana Carolina Arias Cáu, Luciane Zgoda Bussmann, et al.
Journal of Bone and Mineral Metabolism|July 7, 2023
Evaluation of the trabecular bone score in 35 children and adults with X-linked hypophosphatemic ricketsGuido de Paula Colares Neto, Rosa Maria Rodrigues Pereira, Jackeline Couto Alvarenga, et al.
Pediatric Nephrology (Berlin, Germany)|May 12, 2011
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndromeThatiana Evilen da Silva, Mirian Yumie Nishi, Elaine Maria Frade Costa, et al.
Journal of the Endocrine Society|May 9, 2019
Nephrocalcinosis and Nephrolithiasis in X-Linked Hypophosphatemic Rickets: Diagnostic Imaging and Risk FactorsGuido de Paula Colares Neto, Fernando Ide Yamauchi, Ronaldo Hueb Baroni, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|May 4, 2012
Advanced prostate cancer as a cause of oncogenic osteomalacia: an underdiagnosed conditionMilena Perez Mak, Verônica Torres da Costa e Silva, Regina Matsunaga Martin, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|July 7, 2009
Analysis of glucose-dependent insulinotropic peptide receptor (GIPR) and luteinizing hormone receptor (LHCGR) expression in human adrenocortical hyperplasiaMarcia Helena Soares Costa, Sorahia Domenice, Ana Claudia Latronico, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Arquivos Brasileiros De Endocrinologia E Metabologia|May 21, 2010
Bone quality and osteoporosis therapyRegina Matsunaga Martin, Pedro Henrique S Correa
Bone|February 9, 2016
Failure of tooth eruption and brachydactyly in pseudohypoparathyroidism are not related to plasma parathyroid hormone-related protein levelsMariana Tenorio Antunes Reis, Diogo Toledo Matias, Maria Estela Justamante de Faria, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levelsMariana Tenorio Antunes Reis, Andreina Cattani, Berenice Bilharinho Mendonca, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|July 20, 2025
Brown tumor of hyperparathyroidism in the maxillofacial region: a retrospective study with 19 patientsBeatriz Afonso Chiliti, Regina Matsunaga Martin, Alan Roger Santos-Silva, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|April 7, 2011
New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT)Luiza Souza Rodrigues, Ana Carolina Arias Cáu, Luciane Zgoda Bussmann, et al.
Journal of Bone and Mineral Metabolism|July 7, 2023
Evaluation of the trabecular bone score in 35 children and adults with X-linked hypophosphatemic ricketsGuido de Paula Colares Neto, Rosa Maria Rodrigues Pereira, Jackeline Couto Alvarenga, et al.
Pediatric Nephrology (Berlin, Germany)|May 12, 2011
A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndromeThatiana Evilen da Silva, Mirian Yumie Nishi, Elaine Maria Frade Costa, et al.
Journal of the Endocrine Society|May 9, 2019
Nephrocalcinosis and Nephrolithiasis in X-Linked Hypophosphatemic Rickets: Diagnostic Imaging and Risk FactorsGuido de Paula Colares Neto, Fernando Ide Yamauchi, Ronaldo Hueb Baroni, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|May 4, 2012
Advanced prostate cancer as a cause of oncogenic osteomalacia: an underdiagnosed conditionMilena Perez Mak, Verônica Torres da Costa e Silva, Regina Matsunaga Martin, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|July 7, 2009
Analysis of glucose-dependent insulinotropic peptide receptor (GIPR) and luteinizing hormone receptor (LHCGR) expression in human adrenocortical hyperplasiaMarcia Helena Soares Costa, Sorahia Domenice, Ana Claudia Latronico, et al.
Pageof 3