Results 41 to 50 of about 1,385 (184)
Update on Membranoproliferative GN [PDF]
, 2014 Membranoproliferative GN represents a pattern of injury seen on light microscopy. Historically, findings on electron microscopy have been used to further subclassify this pathologic entity.
Fishbane, S., Jhaveri, K. D., Masani, N.
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Neurological Peculiarities of POEMS Syndrome: Experience From a Brazilian University Center
Muscle &Nerve, Volume 73, Issue 3, Page 421-426, March 2026.ABSTRACT Aim Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome associated with significant neurologic morbidity. Better understanding of the manifestations of this disease is crucial to early diagnosis and improvement of prognosis.
Renan Fabri Rosenstein +5 more
wiley +1 more source
La periodontitis como factor de riesgo en los pacientes con cardiopatía isquémica [PDF]
, 2004 La patología cardiovascular y en especial la cardiopatía isquémica (CI) se encuentran entre las principales causas de muerte en el mundo occidental. Recientemente se ha incrementado el interés en investigar la relación entre la cardiopatía isquémica y ...
Berini Aytés, Leonardo +3 more
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Journal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.ABSTRACT Background and Aims Monoclonal gammopathy of undetermined significance (MGUS) occurs in some patients with chronic inflammatory demyelinating polyneuropathy (CIDP), but its impact on clinical phenotype and treatment response remains unclear.
R. van Veen +16 more
wiley +1 more source
Biclonal Gammopathy in Chronic Lymphocytic Leukemia: Case Report and Review of the Literature
Oman Medical Journal, 2015 Monoclonal gammopathies are frequently seen in B-cell malignancies. Monoclonal proteins are seen in a significant proportion of patients with chronic lymphocytic leukemia (CLL), which is a clonal disorder of mature B cells.
Nafila Al-Riyami +5 more
doaj +1 more source
Miopatía por cuerpos de inclusión: caso clínico y revisión de la literatura [PDF]
, 2013 La miositis por cuerpos de inclusión (MCI) es una patología poco común que se presenta en individuos mayores de 50 años y con mayor frecuencia en hombres, sin embargo, los síntomas pueden empezar 20 años antes de su diagnóstico. Hasta un 30% de los casos
Bautista Molano, Wilson Armando +1 more
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Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT This case report highlights a rare occurrence of osteomalacia induced by hypophosphatemia secondary to ferric carboxymaltose (FCM) therapy in a patient with hereditary hemorrhagic telangiectasia (HHT, or Rendu‐Osler‐Weber syndrome). A 21‐year‐old man presented with left tibial pain without prior trauma, accompanied by severe hypophosphatemia ...
Ioannis S. Vasios +4 more
wiley +1 more source
Interference of M-protein on prothrombin time test – case report. [PDF]
, 2016 The aim of this report was to present a case of interference on prothrombin time (PT) test that directed further laboratory diagnostics and resulted with final detection of monoclonal gammopathy in an 88-year old man.
Ines Vukasović +4 more
core +2 more sources
Genetic susceptibility and pharmacogenetics of Multiple Myeloma [PDF]
, 2011 Multiple Myeloma (MM) is a hematological neoplasm that represent about 1% of all hematological malignancies. Several evidences have suggested the presence of genetic factor able to confer susceptibility to MM.
MARTINO, ALESSANDRO
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Differential Rheology Among ABO Blood Group System In Nigerians [PDF]
, 2016 Background: ABO blood groups have been reported to have rheological significance and association with different disease conditions. The non-O blood groups (A, B, and AB) have shown more susceptibility to arterial and venous thrombotic diseases with no ...
Ajayi, OI, Ekakitie, OO, Okpalaugo, OC
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