Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Muralee Dharan"'
Autor:
Michelle Dubb, Petra Macaskill, Ravirani Samuel, Manar Khalid, Massimo Bongiovanni, Laura Criado, Guang-Ping Wu, Alfredo Pontecorvi, Anna Ioakim-Liossi, Elena Aguirregoicoa, Dulce Lorence, Takako Kawada, Esther Diana Rossi, Clare Biro, Keizou Nakayama, Leocardea Schroeter, Marco Raffaelli, Rajpal Singh Punia, Sudhir Garg, Dimitra Grapsa, Mohan H. Kulkarni, Ondrej Hes, Muralee Dharan, Gloria Duane, Guido Fadda, Rose Venegas, Neeta Kumar, Prakash R. Malur, Suzanne Hyne, Shahidul Islam, Susan J. Robertson, Panagiota Mikou, Antonino Mulè, Efthalia Petrakakou, Ma Jesús Fernández-Aceñero, Nausheen Yaqoob, Naoto Kuroda, Julia K. Thurloe, Harsh Mohan, Cinzia Anna Maria Calla, Joanne Clarke, Elizabeth Davey, Dalal Nemenqani, Pamela Michelow, Chang-Qing Fang, Mercia Louw, Rajakumar D. Mastiholimath, Jean-Claude Pache, Brad P. Barnett, Dimitris Tsarpalis, Nicolas Guillaume, Shu-Li Liu, Momein Hafiz, Jean-François Claisse, Celestino Pio Lombardi, Mohamed Osman Kamal, Barbara De Saussure, Aris Polyzos, Sheila Sheth, Sevgiye Kaçar Özkara, Hema B Bannur, Vamseedhar Annam, Iris Teo, Wayne Grayson, Sujatha S. Giriyan, Jean-Claude Capiod, Yoshiaki Imamura, Syed Z. Ali, Maria-Efi Stergiou, Iona Vaida, Colleen Wright, Badr AbdullGaffar, Anna Giahnaki, Kien T. Mai, Shakil H. Merchant, Edmund S. Cibas, Ying Sun, Rafeea AlGhufli, Les Irwig, Gian Franco Zannoni, Alan Rubin, Peter A.B. Wranz, Gupse Turan, Hossein M. Yazdi, Tadanori Yamaguchi, Uma Handa, Celia Marginean, Mehrvash Haghighi, Boris Shlopov, Niti Singhal
Publikováno v:
Acta Cytologica. 53:727-738
Autor:
Muralee Dharan
Publikováno v:
Acta Cytologica. 49:101-104
Background Primary colloid or mucinous carcinoma of the salivary glands is extremely rare. Only a few cases have been reported that originated in the minor salivary glands. an even more exceptional presentation is as a metastatic tumor in the parotid
Publikováno v:
Hormone Research in Paediatrics. 62:23-26
Objective: A patient is reported with hypertension due to combined medullary adrenal hyperplasia and myelolipoma. Methods: A 52-year-old woman with long-standing hypertension was evaluated for an incidentally discoveredlargetumor of the left adrenal.
Publikováno v:
The Endocrinologist. 19:55-57
Publikováno v:
Acta Cytologica. 42:791-795
BACKGROUND: Synovial sarcoma (SS), a malignant mesenchymal tumor, has a biphasic growth pattern characteristically. Histologically and cytologically the tumor can pose diagnostic difficulty when the epithelial component is predominant. CASE REPORT: A
Publikováno v:
The American Journal of the Medical Sciences. 331:274-276
A 68-year-old man reported upper abdominal pain during the previous 3 months that worsened in the last 2 days. He had a history of lung squamous cell carcinoma for which he underwent right lung lobectomy 3 years earlier. Preliminary blood tests showe
Publikováno v:
Clinical Endocrinology. 47:613-617
We describe two male patients, aged 17 and 47 years, with clinical and biochemical features of pheochromocytoma. Both patients had normal-sized adrenal glands on abdominal CT scan and abnormal unilateral uptake of I-123 metaiodobenzylguanidine (MIBG)
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:977-981
Recently, we demonstrated that melatonin secretion was increased in male patients with GnRH deficiency and decreased to normal levels during testosterone treatment. These data suggested that gonadal steroids modulate melatonin secretion, probably by
Autor:
Muralee Dharan, Rafael Luboshitzky
Publikováno v:
Diagnostic Cytopathology. 30:122-124
We report on a 35-yr-old woman presenting with a single thyroid nodule. Fine-needle aspiration (FNA) of the nodule was reported to contain both follicular and parafollicular cells. The biphasic nature of the tumor was highlighted on immunohistochemic
Publikováno v:
Clinical Nuclear Medicine. 20:37-41
Two patients with unusual Hodgkin's disease who initially had a painless, solitary, thyroid cold nodule are described. Fine-needle aspiration revealed lymphocytic thyroiditis in one patient and a diagnosis of Hodgkin's disease was made 1 year later.