Results 111 to 120 of about 20,564 (250)
گزارش يک مورد نشانگان پوئمز (POEMS SYNDROME) از ايران و مروری بر مقالاتی که در اين زمينه منتشر شده است. [PDF]
سندرم کرو ـ فوکاس (crow-fukas)، تاکاتسوکی (takatsuki) يا نشانگان پوئمز (POEMS syndrome) که نام آن بر گرفته از ترکيب حروف اول يافتههای بالينی و پاراکلينيکی به لاتين، شامل: پلی نوروپاتی(Polyneuropathy)، ارگانومگالی (Organomegaly)، اندوکرينوپاتی ...
صادقی, حسن اله +1 more
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THE COURSE OF THE DISEASE AND TREATMENT OF TWO PATIENTS WITHPOEMS SYNDROME
BACKGROUND Here are presented two cases of a multisystem disorder called POEMS Syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, M protein and Skin changes).
Irena Umek Bricman, Peter Černelč
doaj
Neonatal cholestasis - Single centre experience in Central India
Background: Neonatal cholestasis syndrome (NCS) is a major cause of morbidity and mortality in infants. The disorder has rarely been studied in centers from Central India.
Mayank Jain +8 more
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BACKGROUND We have presented the patient with POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, M protein, Skin changes) in which peripheral neuropathy wasassociated with monoclonal gammopathy and osteosclerotic myeloma.
Bojana Luštrek, Peter Černelč
doaj
Gaze Palsy, Organomegaly, and Inspiratory Stridor: A Diagnostic Triad [PDF]
Priyanka Madaan +4 more
openaire +2 more sources
Treatment of hairy cell leukemia with cladribine (2-chlorodeoxyadenosine) by subcutaneous bolus injection: a phase II study [PDF]
Background: To assess the activity and toxicity of 2-chlorodeoxyadenosine (cladribine, CDA) given by subcutaneous bolus injections to patients with hairy cell leukemia (HCL).
Betticher, D. +15 more
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Icteric flare of chronic hepatitis B in a 95-year old patient [PDF]
A 95-year old gentleman developed fatal icteric flare of chronic hepatitis B despite lamivudine treatment. This article highlights the atypical presentations of chronic hepatitis B in elderly patient and the need to consider this possibility for acute ...
Chan, HLY, Leung, WK, Wong, WS
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[Polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes: the POEMS syndrome].
We present a case of an unusual multi-systematic disorder whose cardinal signs were severe progressive sensorimotor polyneuropathy, hepatomegaly, endocrinopathy, plasma cell dyscrasia with osteosclerotic bone lesions and M-protein production as well as skin lesions (termed POEMS Syndrome) whose pathophysiology is still unknown, as well as its ...
A, Lesić +5 more
openaire +1 more source
Background: Idiopathic multicentric Castleman disease (iMCD) with TAFRO syndrome (characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis/renal failure, organomegaly) is a recently described disorder. The diagnostic criteria for iMCD-TAFRO
Maria Carolina Carvalho +3 more
doaj +1 more source
Plexogenic pulmonary hypertension associated with POEMS syndrome
Pulmonary hypertension is one of the well-known clinical manifestations of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome, occurring in approximately 25–30% of the affected individuals. However, the
Thomas Czeczok, Peter Lin, Eunhee Yi
doaj +1 more source

