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Julio Abucham
Julio Abucham
Professor de Medicina
Verifierad e-postadress på unifesp.br
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Pasireotide versus continued treatment with octreotide or lanreotide in patients with inadequately controlled acromegaly (PAOLA): a randomised, phase 3 trial
MR Gadelha, MD Bronstein, T Brue, M Coculescu, M Fleseriu, ...
The lancet Diabetes & endocrinology 2 (11), 875-884, 2014
3842014
Hypothalamic involvement in chronic migraine
MFP Peres, MS Del Rio, MLV Seabra, S Tufik, J Abucham, J Cipolla-Neto, ...
Journal of Neurology, Neurosurgery & Psychiatry 71 (6), 747-751, 2001
3102001
Conservative management of pituitary apoplexy: a prospective study
P Maccagnan, CL Macedo, MJ Kayath, RG Nogueira, J Abucham
The Journal of Clinical Endocrinology & Metabolism 80 (7), 2190-2197, 1995
2391995
Challenges in the diagnosis and management of acromegaly: a focus on comorbidities
A Abreu, AP Tovar, R Castellanos, A Valenzuela, CMG Giraldo, ...
Pituitary 19, 448-457, 2016
1792016
The impact of sleep on age-related sarcopenia: Possible connections and clinical implications
RD Piovezan, J Abucham, RVT Dos Santos, MT Mello, S Tufik, D Poyares
Ageing research reviews 23, 210-220, 2015
1452015
Controversial issues in the management of hyperprolactinemia and prolactinomas–An overview by the Neuroendocrinology Department of the Brazilian Society of Endocrinology and …
L Vilar, J Abucham, JL Albuquerque, LA Araujo, MF Azevedo, ...
Archives of endocrinology and metabolism 62, 236-263, 2018
1252018
Changes in serum thyroid hormones levels and their mechanisms during long‐term growth hormone (GH) replacement therapy in GH deficient children
ES Portes, JHA Oliveira, P Maccagnan, J Abucham
Clinical Endocrinology 53 (2), 183-189, 2000
992000
Reversible Kallmann syndrome: report of the first case with a KAL1 mutation and literature review
RS Ribeiro, TC Vieira, J Abucham
European Journal of Endocrinology 156 (3), 285-290, 2007
942007
Investigating the paradox of hypothyroidism and increased serum thyrotropin (TSH) levels in Sheehan’s syndrome: characterization of TSH carbohydrate content and bioactivity
JHA Oliveira, L Persani, P Beck-Peccoz, J Abucham
The Journal of Clinical Endocrinology & Metabolism 86 (4), 1694-1699, 2001
792001
Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene
C Asteria, JH Oliveira, J Abucham, P Beck-Peccoz
European journal of endocrinology 143 (3), 347-352, 2000
732000
Short-and long-term efficacy of combined cabergoline and octreotide treatment in controlling IGF-I levels in acromegaly
P Mattar, MR Alves Martins, J Abucham
Neuroendocrinology 92 (2), 120-127, 2010
582010
Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency
TC Vieira, VT Boldarine, J Abucham
Arquivos Brasileiros de Endocrinologia & Metabologia 51, 1097-1103, 2007
562007
Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay
TC Vieira, MR Dias da Silva, JM Cerutti, E Brunner, M Borges, LT Arnaldi, ...
The Journal of Clinical Endocrinology & Metabolism 88 (1), 38-44, 2003
562003
Acromegaly and pregnancy: a prospective study
M Dias, C Boguszewski, M Gadelha, L Kasuki, N Musolino, JGH Vieira, ...
European journal of endocrinology 170 (2), 301-310, 2014
502014
Recovery of persistent hypogonadism by clomiphene in males with prolactinomas under dopamine agonist treatment
RS Ribeiro, J Abucham
European journal of endocrinology 161 (1), 163-169, 2009
492009
Acromegaly and pregnancy: a contemporary
J Abucham, MD Bronstein, ML Dias
European Journal of Endocrinology 177, R1-R12, 2017
472017
Growth hormone replacement improves thyroxine biological effects: implications for management of central hypothyroidism
MRA Martins, FC Doin, WR Komatsu, TL Barros-Neto, VA Moises, ...
The Journal of Clinical Endocrinology & Metabolism 92 (11), 4144-4153, 2007
442007
Hereditary corticosteroid‐binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred
E Brunner, J Baima, TC Vieira, JGH Vieira, J Abucham
Clinical endocrinology 58 (6), 756-762, 2003
422003
Recommendations of Neuroendocrinology Department from Brazilian Society of Endocrinology and Metabolism for diagnosis and treatment of acromegaly in Brazil
L Vieira Neto, J Abucham, LA Araujo, CL Boguszewski, MD BRONSTEIN, ...
Arquivos Brasileiros de Endocrinologia e Metabologia, 2011
402011
Machine learning-based prediction model for treatment of acromegaly with first-generation somatostatin receptor ligands
LE Wildemberg, AH da Silva Camacho, RL Miranda, PCL Elias, ...
The Journal of Clinical Endocrinology & Metabolism 106 (7), 2047-2056, 2021
372021
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Artiklar 1–20