Cargando…

Pediatric CIDP: Diagnosis and Management. A Single-Center Experience

Background: Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare acquired polyneuropathy that especially among youngest children should be differentiated with hereditary neuropathies. Even though upon diagnosis treatment options are similar in children and adults, diagnostic challenges...

Descripción completa

Detalles Bibliográficos
Autores principales:	Łukawska, Małgorzata, Potulska-Chromik, Anna, Lipowska, Marta, Hoffman-Zacharska, Dorota, Olchowik, Beata, Figlerowicz, Magdalena, Kanabus, Karolina, Rosiak, Edyta, Kostera-Pruszczyk, Anna
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284159/ https://www.ncbi.nlm.nih.gov/pubmed/34276534 http://dx.doi.org/10.3389/fneur.2021.667378

Ejemplares similares

Corrigendum: Pediatric CIDP: Diagnosis and Management. A Single-Center Experience
por: Łukawska, Małgorzata, et al.
Publicado: (2022)

Acute Autonomic Neuropathy as a Rare Cause of Severe Arterial Hypertension in a Child
por: Kamińska, Halszka, et al.
Publicado: (2021)

Determinants of Quality of Life in Myasthenia Gravis Patients
por: Szczudlik, Piotr, et al.
Publicado: (2020)

Long lasting dysautonomia due to botulinum toxin B poisoning: clinical- laboratory follow up and difficulties in initial diagnosis
por: Potulska-Chromik, Anna, et al.
Publicado: (2013)

Long-term nusinersen treatment across a wide spectrum of spinal muscular atrophy severity: a real-world experience
por: Łusakowska, Anna, et al.
Publicado: (2023)

BAG3-related myopathy, polyneuropathy and cardiomyopathy with long QT syndrome
por: Kostera-Pruszczyk, Anna, et al.
Publicado: (2015)

Treatment Approaches for Atypical CIDP
por: Menon, Deepak, et al.
Publicado: (2021)

Genomic instability in the PARK2 locus is associated with Parkinson’s disease
por: Ambroziak, Wojciech, et al.
Publicado: (2015)

The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseases
por: Sinkiewicz-Darol, Elena, et al.
Publicado: (2014)

Editorial: Update on the Diagnosis and Management of CIDP Variants
por: Chroni, Elisabeth, et al.
Publicado: (2021)

Lower BAFF Levels in Myasthenic Patients Treated with Glucocorticoids
por: Sobieszczuk, Ewa, et al.
Publicado: (2021)

Abnormality of multimodal evoked potentials in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)
por: Dziadkowiak, Edyta, et al.
Publicado: (2020)

The Cost Effectiveness of Immunoglobulin vs. Hematopoietic Stem Cell Transplantation for CIDP
por: Burt, Richard K., et al.
Publicado: (2021)

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) in Diabetes Mellitus: A Diagnostic Dilemma
por: Valentin, Marcos, et al.
Publicado: (2022)

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): Overview, Treatment, and a Case Study
por: Ponnala, Madhusudhan, et al.
Publicado: (2023)

Individualizing Therapy in CIDP: A Mini-Review Comparing the Pharmacokinetics of Ig With SCIg and IVIg
por: Beydoun, Said R., et al.
Publicado: (2021)

Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients
por: Potulska-Chromik, Anna, et al.
Publicado: (2021)

Lack of miR-378 attenuates muscular dystrophy in mdx mice
por: Podkalicka, Paulina, et al.
Publicado: (2020)

Case Report: Anti-NF186+ CIDP After Receiving the Inactivated Vaccine for Coronavirus Disease (COVID-19)
por: Wen, Shirui, et al.
Publicado: (2022)

Ultra-low radiation dose protocol for CT-guided intrathecal nusinersen injections for patients with spinal muscular atrophy and severe scoliosis
por: Rosiak, Grzegorz, et al.
Publicado: (2021)

Pathophysiology of the Different Clinical Phenotypes of Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)
por: Dziadkowiak, Edyta, et al.
Publicado: (2021)

The comparison of MRN, electrophysiology and progression among typical CIDP and atypical CIDP subtypes
por: Feng, Yuan, et al.
Publicado: (2020)

Vertigo and Severe Balance Instability as Symptoms of Lyme Disease—Literature Review and Case Report
por: Jozefowicz-Korczynska, Magdalena, et al.
Publicado: (2019)

Real World Evidence on the Effectiveness of Nusinersen within the National Program to Treat Spinal Muscular Atrophy in Poland
por: Krupa, Dominika, et al.
Publicado: (2023)

The Misdiagnosis of CIDP: A Review
por: Allen, Jeffrey A.
Publicado: (2020)

Prevalence and impact of autoimmune thyroid disease on myasthenia gravis course
por: Kubiszewska, Justyna, et al.
Publicado: (2016)

Severe CIDP-MGUS responsive to Rituximab
por: Posa, Andreas, et al.
Publicado: (2020)

CIDP mimics: a case series
por: Moshe-Lilie, Orly, et al.
Publicado: (2021)

The neurophysiological lesson from the Italian CIDP database
por: Spina, Emanuele, et al.
Publicado: (2021)

Propafenone is not effective for severe ventricular arrhythmias in Andersen-Tawil syndrome
por: Bienias, Piotr, et al.
Publicado: (2016)

MRI biomarkers of proximal nerve injury in CIDP
por: Lichtenstein, Thorsten, et al.
Publicado: (2017)

Progress in Hematopoietic Stem Cell Transplantation for CIDP
por: Qin, Zhen, et al.
Publicado: (2020)

Targeted Next-Generation Sequencing Reveals Mutations in Non-coding Regions and Potential Regulatory Sequences of Calpain-3 Gene in Polish Limb–Girdle Muscular Dystrophy Patients
por: Macias, Anna, et al.
Publicado: (2021)

Genetic Risk Factors for Neurological Disorders in Children with Adverse Events following Immunization: A Descriptive Study of a Polish Case Series
por: Charzewska, Agnieszka, et al.
Publicado: (2023)

Evaluation of the EFNS/PNS diagnostic criteria in a cohort of CIDP patients
por: Athanasopoulos, Diamantis, et al.
Publicado: (2021)

Deregulated Fcγ receptor expression in patients with CIDP
por: Quast, Isaak, et al.
Publicado: (2015)

CIDP prognosis in patients with IVIG treatment‐related fluctuations
por: Cook, Melissa, et al.
Publicado: (2022)

Gross Motor Function Disorders in Patients with Alternating Hemiplegia of Childhood
por: Stępień, Agnieszka, et al.
Publicado: (2020)

Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients
por: Fichna, Jakub Piotr, et al.
Publicado: (2018)

Progressive External Ophthalmoplegia in Polish Patients—From Clinical Evaluation to Genetic Confirmation
por: Kierdaszuk, Biruta, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_osqbvni7mpq2r0f1q1u3327mbc