Departamento de Ciencias Forenses, Anatomía Patológica, Ginecología y Obstetricia y Pediatría
Departamento
Hospital de São João
Oporto, PortugalPublicaciones en colaboración con investigadores/as de Hospital de São João (49)
2020
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Ibero-latinamerican clinical practical guidelines on pediatric caustic esophagitis: Physiopathology and clinical-endoscopic diagnosis (1st part)
Revista Chilena de Pediatria, Vol. 91, Núm. 1, pp. 149-157
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Long-term effects of medical management on growth and weight in individuals with urea cycle disorders
Scientific Reports, Vol. 10, Núm. 1
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Pitfalls in Challenging Thyroid Tumors: Emphasis on Differential Diagnosis and Ancillary Biomarkers
Endocrine Pathology, Vol. 31, Núm. 3, pp. 197-217
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Tumors of the thyroid gland. Proposal for the management and study of samples from patients with thyroid neoplasms
Revista Espanola de Patologia, Vol. 53, Núm. 1, pp. 27-36
2019
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Newborn screening for homocystinurias: Recent recommendations versus current practice
Journal of Inherited Metabolic Disease, Vol. 42, Núm. 1, pp. 128-139
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Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—A successful strategy for clinical research of rare diseases
Journal of Inherited Metabolic Disease, Vol. 42, Núm. 1, pp. 93-106
2018
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Correction to: Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders (Journal of Inherited Metabolic Disease, (2016), 39, 5, (661-672), 10.1007/s10545-016-9938-9)
Journal of Inherited Metabolic Disease
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Correction to: Impact of age at onset and newborn screening on outcome in organic acidurias (Journal of Inherited Metabolic Disease, (2016), 39, 3, (341-353), 10.1007/s10545-015-9907-8)
Journal of Inherited Metabolic Disease
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Cribriform-morular variant of thyroid carcinoma: a neoplasm with distinctive phenotype associated with the activation of the WNT/β-catenin pathway
Modern Pathology, Vol. 31, Núm. 8, pp. 1168-1179
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New WHO classification of thyroid tumors: a pragmatic categorization of thyroid gland neoplasms
Endocrinologia, Diabetes y Nutricion, Vol. 65, Núm. 3, pp. 133-135
2017
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EWSR1 rearrangement is a frequent event in papillary thyroid carcinoma and in carcinoma of the thyroid with Ewing family tumor elements (CEFTE)
Virchows Archiv, Vol. 470, Núm. 5, pp. 517-525
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Hobnail variant of papillary thyroid carcinoma: Clinicopathologic and molecular evidence of progression to undifferentiated carcinoma in 2 cases
American Journal of Surgical Pathology, Vol. 41, Núm. 6, pp. 854-860
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Other rare tumours and tumour-like lesions
Rare Tumors of the Thyroid Gland: Diagnosis and WHO Classification (Springer International Publishing), pp. 79-105
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Rare familial tumours
Rare Tumors of the Thyroid Gland: Diagnosis and WHO Classification (Springer International Publishing), pp. 57-77
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Rare follicular tumours
Rare Tumors of the Thyroid Gland: Diagnosis and WHO Classification (Springer International Publishing), pp. 27-44
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Rare papillary thyroid carcinomas
Rare Tumors of the Thyroid Gland: Diagnosis and WHO Classification (Springer International Publishing), pp. 5-25
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Small cell tumours
Rare Tumors of the Thyroid Gland: Diagnosis and WHO Classification (Springer International Publishing), pp. 45-56
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TERT, BRAF, and NRAS in primary thyroid cancer and metastatic disease
Journal of Clinical Endocrinology and Metabolism, Vol. 102, Núm. 6, pp. 1898-1907
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Therapeutic options
Rare Tumors of the Thyroid Gland: Diagnosis and WHO Classification (Springer International Publishing), pp. 107-110
2016
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Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders
Journal of Inherited Metabolic Disease, Vol. 39, Núm. 5, pp. 661-672