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Repurposing Saquinavir for Host-Directed Therapy to Control Mycobacterium Tuberculosis Infection

Frontiers in immunology, 2021-03, Vol.12, p.647728

2021

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Fat Distribution and Lipid Profile of Young Adults with Congenital Adrenal Hyperplasia Due to 21‐Hydroxylase Enzyme Deficiency

Lipids, 2021-01, Vol.56 (1), p.101-110

2021

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Systematic review of quality of life in Turner syndrome

Quality of life research, 2018-08, Vol.27 (8), p.1985-2006

2018

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Dies1/VISTA expression loss is a recurrent event in gastric cancer due to epigenetic regulation

Scientific reports, 2016-10, Vol.6 (1), p.34860-34860, Article 34860

2016

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Higher Body Fat but Similar Phase Angle Values in Patients with the Classical Form of Congenital Adrenal Hyperplasia in Comparison to a Control Group

Nutrients, 2022-12, Vol.14 (23), p.5184

2022

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The bone densitometry is normal in Turner syndrome prepubertal patients after height age correction

Revista Brasileira de Saúde Materno Infantil, 2021-12, Vol.21 (4), p.1129-1134

2021

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Coastal climate adaptation in port-cities: adaptation deficits, barriers, and challenges ahead

Journal of environmental planning and management, 2020-02, Vol.63 (3), p.389-414

2020

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Normal bone health in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy

Osteoporosis international, 2022, Vol.33 (1), p.283-291

2022

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A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins

Diabetology and metabolic syndrome, 2015-11, Vol.7 (96), p.101, Article 101

2015

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Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiency

Nutrition (Burbank, Los Angeles County, Calif.), 2012-10, Vol.28 (10), p.984-990

2012

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TIM-3 Is a Potential Immune Checkpoint Target in Cats with Mammary Carcinoma

Cancers, 2023-01, Vol.15 (2), p.384

2023

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Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia

Clinical biochemistry, 2019-11, Vol.73, p.50-56

2019

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Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density

Journal of bone and mineral metabolism, 2003-01, Vol.21 (6), p.396-401

2003

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Turner syndrome and metabolic derangements: Another example of fetal programming

Early human development, 2012-02, Vol.88 (2), p.99-102

2012

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Bioelectrical Impedance Phase Angle and Its Determinants in Patients with Classic Congenital Adrenal Hyperplasia

Journal of the American College of Nutrition, 2022-05, Vol.ahead-of-print (ahead-of-print), p.1-8

2022

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Growth charts of Brazilian girls with Turner syndrome without the use of GH or oxandrolone

Jornal de pediatria, 2024-10

2024

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Does phonological overlap of cognate words modulate cognate acquisition and processing in developing and skilled readers?

Language acquisition, 2018-10, Vol.25 (4), p.438-453

2018

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Clinical and laboratory profile of pediatric and adolescent patients with type 1 diabetes

Jornal de pediatria, 2009-11, Vol.85 (6), p.490-494

2009

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Phenotype of regulatory T cells in human type 1 diabetes at diagnosis and partial remission phase

Diabetology and metabolic syndrome, 2015-11, Vol.7 (S1), p.A208-A208, Article A208

2015

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Turner syndrome and metabolic derangements: Another example of fetal programing

Early human development, 2012, Vol.88 (2), p.99-102

2012

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Observação sistemática dos procedimentos da equipe de enfermagem na coleta de urina para cultura

Revista da Escola de Enfermagem da U S P, 1980-12, Vol.14 (3), p.337-337

Sofia, M.T.B. Valente

1980

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Perfil clínico e laboratorial de pacientes pediátricos e adolescentes com diabetes tipo 1 Clinical and laboratory profile of pediatric and adolescent patients with type 1 diabetes

Jornal de pediatria, 2009-12, Vol.85 (6), p.490-494

2009

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Perfil clínico e laboratorial de pacientes pediátricos e adolescentes com diabetes tipo 1

Jornal de pediatria, 2009-12, Vol.85 (6), p.490-494

2009

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Perfil clínico e laboratorial de pacientes pediátricos e adolescentes com diabetes tipo 1

Jornal de pediatria, 2009-12, Vol.85 (6), p.490-494

2009

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ESTUDO SOBRE COLHEITA DE URINA PARA CULTURA

Revista da Escola de Enfermagem da U S P, 1983-12, Vol.17 (3), p.253-274

Valente, Sofia Maria Taffil Bello

1983

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Repurposing Saquinavir for Host-Directed Therapy to Control Mycobacterium Tuberculosis Infection

Fat Distribution and Lipid Profile of Young Adults with Congenital Adrenal Hyperplasia Due to 21‐Hydroxylase Enzyme Deficiency

Systematic review of quality of life in Turner syndrome

Dies1/VISTA expression loss is a recurrent event in gastric cancer due to epigenetic regulation

Higher Body Fat but Similar Phase Angle Values in Patients with the Classical Form of Congenital Adrenal Hyperplasia in Comparison to a Control Group

The bone densitometry is normal in Turner syndrome prepubertal patients after height age correction

Coastal climate adaptation in port-cities: adaptation deficits, barriers, and challenges ahead

Normal bone health in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy

A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins

Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiency

TIM-3 Is a Potential Immune Checkpoint Target in Cats with Mammary Carcinoma

Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia

Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density

Turner syndrome and metabolic derangements: Another example of fetal programming

Bioelectrical Impedance Phase Angle and Its Determinants in Patients with Classic Congenital Adrenal Hyperplasia

Growth charts of Brazilian girls with Turner syndrome without the use of GH or oxandrolone

Does phonological overlap of cognate words modulate cognate acquisition and processing in developing and skilled readers?

Clinical and laboratory profile of pediatric and adolescent patients with type 1 diabetes

Phenotype of regulatory T cells in human type 1 diabetes at diagnosis and partial remission phase

Turner syndrome and metabolic derangements: Another example of fetal programing

Observação sistemática dos procedimentos da equipe de enfermagem na coleta de urina para cultura

Perfil clínico e laboratorial de pacientes pediátricos e adolescentes com diabetes tipo 1 Clinical and laboratory profile of pediatric and adolescent patients with type 1 diabetes

Perfil clínico e laboratorial de pacientes pediátricos e adolescentes com diabetes tipo 1

Perfil clínico e laboratorial de pacientes pediátricos e adolescentes com diabetes tipo 1

ESTUDO SOBRE COLHEITA DE URINA PARA CULTURA

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