Results 21 to 30 of about 39,459 (267)

Serum catestatin level in preeclampsia [PDF]

open access: yesScripta Medica
Background/Aim: Preeclampsia, a significant cause of maternal morbidity and mortality, is linked to increased cardiovascular risks. Catestatin regulates cardiovascular function which indicates its usefulness in understanding pathophysiology of ...
Alghazali Basima Sh, Tabarak Karim Mahdi
doaj   +1 more source

Metastasizing esthesioneuroblastoma in a dog [PDF]

open access: yes, 2014
A 7-year-old Afghan hound presented with a history of disorientation, loss of vision, and seizures. Magnetic resonance imaging helped identify a mass at the level of the main olfactory bulb that compressed and displaced adjacent tissues in the cribriform
Herden, Christiane   +3 more
core   +1 more source

Genetic background influences tumour development in heterozygous Men1 knockout mice [PDF]

open access: yes, 2020
Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disorder caused by MEN1 germline mutations, is characterised by parathyroid, pancreatic and pituitary tumours. MEN1 mutations also cause familial isolated primary hyperparathyroidism (FIHP)
Christie, Paul T.   +11 more
core   +2 more sources

Neuroendocrine Carcinoma of the Stomach-A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Neuroendocrine carcinomas of stomach have been considered a rare neoplasm. The present case concerns with a 69 year old male, who presented with vague abdominal discomfort and history of malena.
Poorana Priya P.   +2 more
doaj   +1 more source

Unusual Presentation of Primary Ovarian Carcinoid Tumours with Low-toModerate Proliferative Potential [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2020
Primary Ovarian Carcinoid Tumour (OCT) are rare benign neuroendocrine neoplasms. Herewith, two cases of ovarian tumour has been described. In case 1, patient was a 63-year-old postmenopausal woman with vague abdominal pain.
Supriya Mehrotra   +4 more
doaj   +1 more source

Chromogranin A and chromogranin B in pancreatic neuroendocrine tumors

open access: yesMedical alphabet, 2020
For the first time in Russia a comparative study of chromogranin A (CgA) and chromogranin B (CgB) in neuroendocrine tumors (NETs) of the pancreas was performed. We examined 50 primary patients with pancreatic NETs and 42 healthy people. The determination of CgA and CgB was performed in blood serum using standard enzyme-linked immunoassay test-systems ...
N. V. Lyubimova   +3 more
openaire   +2 more sources

Hepatic progenitor cells from adult human livers for cell transplantation. [PDF]

open access: yes, 2008
Objective: Liver regeneration is mainly based on cellular self-renewal including progenitor cells. Efforts have been made to harness this potential for cell transplantation, but shortage of hepatocytes and premature differentiated progenitor cells ...
Aurich, H.   +10 more
core   +1 more source

Neoadjuvant chemotherapy with capecitabine and temozolomide for unresectable pancreatic neuroendocrine tumor. [PDF]

open access: yes, 2012
Pancreatic neuroendocrine tumors (PNETs) are relatively rare tumors that arise in the endocrine cells of the pancreas. Historically, somatostatin analogues have been used in this disease primarily for symptom control and, to a limited extent, disease ...
Devata, Sumana, Kim, Edward J
core   +7 more sources

FGFR2 amplification in colorectal adenocarcinoma [PDF]

open access: yes, 2017
FGFR2 is recurrently amplified in 5% of gastric cancers and 1%–4% of breast cancers; however, this molecular alteration has never been reported in a primary colorectal cancer specimen.
Carter, Jamal H   +6 more
core   +2 more sources

Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors [PDF]

open access: yes, 2018
Background. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index.
Baldelli, Roberto   +8 more
core   +1 more source

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