Results 131 to 140 of about 20,564 (250)
Successful Pregnancy Outcome In Maternal Crigler Najjar Syndrome Type II. [PDF]
, 2012 Estimated incidence of Crigler-Najjar syndrome(CNS) is 1 case per 1,000,000 births(1 million). The overall prevalence of CN syndrome is unknown, with only several hundred people reported to have this disease.
Padmalatha, VV +3 more
core
پزشکی بالینی ابن سینا, 2002 POEMS syndrome is a plasmocytic dyscrasia that consists a constellation of polyneuropathy(p), organomegaly(o), endocrinopathy(e), monoclonal gammapathy(m) and skin disorders(s).
Seyyed Davoud Mansoori +2 more
doaj
Efficacy and safety of bortezomib with dexamethasone regimen in elderly newly diagnosed multiple myeloma patients with co-morbidities [PDF]
, 2016 Bortezomib-based induction therapies have shown to increase complete response rates and are used as an upfront therapy for newly diagnosed multiple myeloma patients.
Lee, Saem
core +1 more source
Role of Fine Needle Aspiration Cytology in Salivary Gland Pathology and its Histopathological Correlation: A Two Year Prospective Study in Western India. [PDF]
, 2012 Background and objectives: Salivary gland lesions account for 2-6.5% of all the neoplasms of the head and neck. Fine needle aspiration cytology (FNAC) is being increasingly used in the diagnosis of salivary gland lesions.
Agravat, AH +3 more
core +1 more source
World Journal of Clinical CasesBACKGROUND Polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes (POEMS) syndrome is a rare paraneoplastic syndrome that encompass multiple systems. The most common clinical symptoms of POEMS syndrome are progressive sensorimotor polyneuropathy, organ enlargement, endocrine disorders, darkening skin, a monoclonal plasma cell ...
Li, Jia-Rong +4 more
openaire +2 more sources
Acute massive myelofibrosis with acutelymphoblastic leukemia [PDF]
, 2009 Acute myelofibrosis is characterized by pancytopenia of sudden onset, megakaryocytic hyperplasia, extensive bone marrow fibrosis, and the absence of organomegaly. Acute myelofibrosis in patients with acute lymphoblastic leukemia is extremely rare.
Barış Malbora +5 more
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Journal of Karnali Academy of Health SciencesBackground: Hepatosplenomegaly is the simultaneous enlargement of liver and spleen. Its causes are enteric fever, hepatitis, scrub typhus, acute liver failure and leukemia and so on.
Uttara Gautam +4 more
doaj +1 more source
Multiple Organomegaly Exhibited in a Patient with Graves' Hyperthyroidism
Internal Medicine, 2016 Kazuki, Ocho +2 more
openaire +3 more sources