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Multiple endocrine neoplasia type 2

Clinics  vol.61 número1

Clinics vol.61 número1

... Multiple endocrine neoplasia type 2 (MEN2) is associated with the occurrence of 3 inherited endocrine tumors: medul- lary thyroid carcinoma (MTC), primary hyperparathyroidism ...

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Neoplasia Endócrina Múltipla Tipo 2: Manejo Diagnóstico e Terapêutico.

Neoplasia Endócrina Múltipla Tipo 2: Manejo Diagnóstico e Terapêutico.

... diseases. Endocrine hypertension and a rare syndrome of multiple endocrine neoplasia (MEN) type 2 were ...MEN type 2 are ...Keywords: Multiple ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... of multiple endocrine neoplasia type 2, encompassing medullary thyroid cancer, pheochromocytoma, and primary hyperparathyroidism, which did not emerge before the early ...developing ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... Multiple endocrine neoplasia type 2 is an autosomal-dominant hereditary cancer syndrome caused by missense gain-of-function mutations of the rearranged during transfection ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... of multiple endocrine neoplasia type 2 and a strong genotype-phenotype correlation exists, particularly between a specific RET codon mutation and the (a) age-related onset and (b) ...

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Paragangliomas/pheochromocytomas: clinically oriented genetic testing

Paragangliomas/pheochromocytomas: clinically oriented genetic testing

... (Multiple Endocrine Neoplasia type 2), and NF1 gene (Neurofibromatosis type 1), 10 novel genes have so far been implicated in the occurrence of paragangliomas/pheochromocytomas: ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... as multiple endocrine neoplasia type ...in multiple endocrine neoplasia type 2 cases was recently determined to be ...and multiple endocrine ...

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Early diagnosis of multiple endocrine neoplasia type 2B: a challenge for physicians

Early diagnosis of multiple endocrine neoplasia type 2B: a challenge for physicians

... tiple Endocrine Neoplasia 2A (MEN2A) and 2B ...cases, 2 men and 2 women, with differences in their phenotypes and with a late ...for multiple endocrine neoplasia ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... as multiple endocrine neoplasia type 1 (MEN1), MEN2A, familial isolated hyperparathyroidism, autosomal dominant mild hyperparathyroidism, neonatal severe hyperparathyroidism, familial ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... and multiple endocrine neoplasia (MEN) type 2 A and B syndromes (5–7), among others ...MEN type 2 and medullary thyroid carcinoma ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... ‘‘multiple endocrine neoplasia’’ (MEN) to describe disor- ders featuring combinations of endocrine tumors; they designated the Wermer syndrome as MEN1 and the Sipple syndrome as ...subdivided ...

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MEN1 gene in endocrine and nonendocrine sporadic tumors

MEN1 gene in endocrine and nonendocrine sporadic tumors

... the multiple endocrine neoplasia type 1 (MEN1) syndrome, somatic mutations of the MEN1 gene have also been described in sporadic tumors like gastrinomas, insulinomas and bronchial carcinoid ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... with multiple endocrine neoplasia type 1 (HPT/MEN1) comprises up to ...of endocrine and non-endocrine ...main endocrine glands involved in this syndrome ...the ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at ...

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Clinics  vol.67 suppl.1

Clinics vol.67 suppl.1

... with multiple endocrine neoplasia type 1, and is also the most common ...in multiple endocrine neoplasia type 1/hyperparathyroidism are still under ...

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Arq Bras Endocrinol Metab  vol.56 número8

Arq Bras Endocrinol Metab vol.56 número8

... include multiple endocrine neo- plasia type 1 (MEN1), in which pituitary, parathyroid, and pancreatic tumors might be associated (4), and the similar MEN4 syndrome caused by germline mu- tations in ...

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Arq Bras Endocrinol Metab  vol.54 número8

Arq Bras Endocrinol Metab vol.54 número8

... Apresentamos dados clínicos e moleculares de quatro famílias com adenoma hipofisário fami- liar isolado (FIPA) enfatizando as diferenças na presença ou não de mutação do AIP e a impor- tância da triagem genética. A ...

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Morbillivirus v proteins exhibit multiple mechanisms to block type 1 and type 2 interferon signalling pathways.

Morbillivirus v proteins exhibit multiple mechanisms to block type 1 and type 2 interferon signalling pathways.

... own type 1 IFN, and support the replication of all morbilliviruses, and A549 cells because they have good levels of endogenous STAT1 and STAT2, making immu- nofluorescence visualisation of STAT activation better ...

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Neoplasia endócrina múltipla tipo 2 .

Neoplasia endócrina múltipla tipo 2 .

... O CMT manifesta-se clinicamente como um nódulo ou massa cervical. Em aproximadamente 50% dos casos os pacientes já apresentam comprometi- mento em linfonodos cervicais ao diagnóstico. As me- tástases a distância e os ...

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Sao Paulo Med. J.  vol.124 número6

Sao Paulo Med. J. vol.124 número6

... CASE REPORT A 17-year-old female was admitted to the Endocrinology Service of Hospital de Clínicas in Uberlândia, Minas Gerais, Brazil, with a history of weight gain, excessive hair, acne and secondary amenorrhea that ...

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