Results 41 to 50 of about 1,143 (194)

Neurological Peculiarities of POEMS Syndrome: Experience From a Brazilian University Center

open access: yesMuscle &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

CIDP With and Without Monoclonal Gammopathy of Undetermined Significance (MGUS): Comparison of Clinical Phenotype, Diagnostic Features, and Treatment Response

open access: yesJournal 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

A case of scleromyxedema without monoclonal gammopathy responded to treatment with IVIG [PDF]

open access: yes, 2012
‘‘Liken miksödematozus’’ deride fibroblast artışı ve müsin birikimi ile karakterize primer inflamatuvar bir dermatozdur. Skleromiksödem liken miksödematozusun jeneralize formu olup papüler lezyonlar, difüz skleroz ve eritem ile seyreder.
Sarıcaoğlu, Hayriye   +4 more
core   +4 more sources

Osteomalacia Following Iron Infusion Therapy in a Patient With Rendu‐Osler‐Weber Syndrome: F‐18‐FDG PET/CT Discrimination of a Stress Fracture in the Setting of a Musculoskeletal Tumor Mimic

open access: yesClinical 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

Compresión del plexo lumbosacro por plasmocitoma: mieloma múltiple de cadenas ligeras tipo lambda

open access: yesRevista Médica Herediana, 2015
Se presenta el caso de una mujer de 51 años que desarrolló paraparesia y una masa abdominal palpable más pérdida de peso en el lapso de cuatro meses. La masa destruía la 5ª vértebra lumbar y se extendía a los tejidos blandos adyacentes. En suero se halló
Oscar G. Pamo   +2 more
doaj  

Perfil proteinogramico en sueros de pollos [PDF]

open access: yes, 1983
El presente trabajo de investigación, nos permitirá conocer los valores normales de proteínas séricas en los pollos de engorde de crianza comercial. El determinar los valores normales de las proteínas que constituyen el suero de las aves, en el caso ...
Muñante Acevedo, Luis Gustavo
core  

Clinical Utility of Serum Neurofilament Light Chain in Peripheral Neuropathy

open access: yesMuscle &Nerve, Volume 73, Issue 1, Page 86-92, January 2026.
ABSTRACT Introductions/Aims The clinical utility of serum neurofilament light chain (sNfL) in the evaluation and management of peripheral neuropathy (PN) remains poorly defined. This study aimed to evaluate the utility of sNfL for diagnosing PN, assessing disease activity, and monitoring treatment response using a commercially available assay.
Chafic Karam
wiley   +1 more source

Ultrasound in the Diagnosis of Chronic Inflammatory Demyelinating Polyneuropathy in Patients With Diabetic Neuropathy

open access: yesClinical Neuroimaging, Volume 3, Issue 1, 2026.
ABSTRACT Introduction The diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP) in patients with diabetic sensorimotor polyneuropathy (DSP) is challenging when both diseases coexist, as patients with DSP may have demyelinating features in nerve conduction studies (NCS).
Lucas Immich Gonçalves   +3 more
wiley   +1 more source

A Case Report of Non‐Neutralizing Acquired Factor V Inhibitor Mimicking Deficiency: Diagnostic Challenges and Therapeutic Implications

open access: yesCase Reports in Hematology, Volume 2026, Issue 1, 2026.
Acquired Factor V (FV) deficiency due to inhibitors is a rare coagulopathy that presents significant diagnostic and therapeutic challenges. We report the case of an 81‐year‐old male with persistent gross hematuria and severe coagulopathy, marked by prolonged prothrombin time (PT), activated partial thromboplastin time (aPTT), and critically low FV ...
Shreyas Kalantri   +6 more
wiley   +1 more source

Paraproteinemias igg: caracterización isotipica y correlaciones clinicobiologicas [PDF]

open access: yes, 1992
Cuatrocientos diecisiete pacientes con paraproteinemia (pp) igg o iga fueron estudiados para las siguientes características: isotipo de pp, cuantificación de igs., presencia de bj sérica, grado de polimerización de las ppiga y diagnóstico.
González González, José Bernardino
core  

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