Cargando…

Hyperargininemia Presenting as Intermittent Ataxia and Cerebellar Atrophy

Detalles Bibliográficos
Autores principales:	Cornelius, Leema P., Raju, Vivekasaravanan, Julin, Asir
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2020
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313582/ https://www.ncbi.nlm.nih.gov/pubmed/32606543 http://dx.doi.org/10.4103/aian.AIAN_130_19

Ejemplares similares

Arginase Deficiency Presenting as Acute Encephalopathy
por: Cornelius, Leema Pauline, et al.
Publicado: (2019)

Pediatric Glutaric Aciduria Type 1: 14 Cases, Diagnosis and Management
por: Cornelius, Leema P., et al.
Publicado: (2021)

Cerebral Venous Sinus Thrombosis Following Primary Varicella Infection in a Child
por: Cornelius, Leema P, et al.
Publicado: (2020)

Vertebrobasilar Insufficiency Presenting as Orthostatic Cerebellar Ataxia
por: Kim, Geun Soo, et al.
Publicado: (2021)

Late Diagnosis of Wilson Disease, Initially Presenting as Cerebellar Atrophy Mimicking Spinocerebellar Ataxia, by Multigene Panel Testing
por: Kim, Min-Kyeong, et al.
Publicado: (2020)

A Case of Epilepsia Partialis Continua Due to Linear Nevus Syndrome with Hemimegalencephaly
por: Cornelius, Leema Pauline, et al.
Publicado: (2017)

Upbeat Nystagmus in Late Onset Cerebellar Ataxia: Think of Anti-Glutamate Decarboxylase 65 Antibody-Associated Cerebellar Ataxia
por: Mahale, Rohan R., et al.
Publicado: (2021)

An Unusual Presentation of Cerebellar Ataxia with Bilateral Vestibulopathy Syndrome: A Case Report
por: Alex, Anu, et al.
Publicado: (2020)

Spinocerebellar Ataxia 13 Presenting with Pure Cerebellar Syndrome in a Korean Family
por: Kim, Minkyeong, et al.
Publicado: (2020)

Autosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case report
por: Chang, Kai-Chieh, et al.
Publicado: (2020)

Isolated Bilateral Superior Cerebellar Peduncular Lesion Presenting Square-Wave Jerks and Ataxia
por: Kong, Jooheon, et al.
Publicado: (2023)

Reversible Cerebellar Ataxia Secondary to Carcinoid Tumor
por: Vishnu, Venugopalan Y, et al.
Publicado: (2016)

Neuromelioidosis Presenting as Bells Palsy in a Child
por: Cornelius, Leema P., et al.
Publicado: (2022)

The Rise of Cerebellar Ataxia in South Korea: 2002–2016
por: Park, YoonAh, et al.
Publicado: (2020)

A case of cerebellar ataxia associated with VZV infection
por: Matsuyama, Hirofumi, et al.
Publicado: (2018)

Efavirenz-Induced Delayed Onset Cerebellar Ataxia and Encephalopathy
por: Sarma, GRK, et al.
Publicado: (2022)

Post COVID Acute Cerebellar Ataxia and Myoclonus (ACAM)
por: Maramattom, Boby Varkey, et al.
Publicado: (2022)

Hypergonadotrophic hypogonadism and cerebellar ataxia in an Indian adolescent: A rare report
por: Mahale, Rohan R., et al.
Publicado: (2015)

Hyperargininemia Due to Arginase 1 Deficiency: Variability in Clinical and Biochemical Presentations in Malaysian children
por: Habib, Anasufiza, et al.
Publicado: (2022)

Preeruptive Unilateral Cerebellar Ataxia in an Immunocompetent Adult: A Rare Case of Varicella
por: Ng, Chen Fei, et al.
Publicado: (2018)

Cervical Dystonia with Cerebellar Ataxia in KCNA1 Mutation: A Phenotypic Expansion
por: Mahale, Rohan R., et al.
Publicado: (2022)

Unusual Case of Cerebellopontine Angle Epidermoid Causing Cerebellar Atrophy
por: Rajeev, Rajasekharan, et al.
Publicado: (2018)

Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations
por: Ramsey, Keri, et al.
Publicado: (2022)

Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation
por: Mahale, Rohan R., et al.
Publicado: (2021)

Novel CHP1 mutation in autosomal-recessive cerebellar ataxia: autopsy features of two siblings
por: Saito, Rie, et al.
Publicado: (2020)

Acetyl-DL-leucine improves gait variability in patients with cerebellar ataxia—a case series
por: Schniepp, Roman, et al.
Publicado: (2016)

Anti-metabotropic-glutamate-receptor 2-related encephalitis with cerebellar ataxia: a case description
por: Li, Dezheng, et al.
Publicado: (2023)

Successful Treatment of Basilar Invagination and Platybasia Associated With Cerebellar Atrophy by Decompression Surgery
por: Lee, Juhee, et al.
Publicado: (2022)

Untreated anti-Ca/ARHGAP26 autoantibody-associated cerebellar ataxia progressing over 27 years
por: Schegk, E., et al.
Publicado: (2023)

The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children
por: Terracciano, Alessandra, et al.
Publicado: (2012)

Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs
por: Christen, Matthias, et al.
Publicado: (2021)

Spinocerebellar Ataxia 28 Presenting as Predominantly Generalized Dystonia
por: Raj, Jidhin, et al.
Publicado: (2021)

Anesthetic considerations in a patient with multiple system atrophy-cerebellar for lower limb surgery
por: Agarwal, Sandhya, et al.
Publicado: (2017)

Postural Ataxia in Cerebellar Downbeat Nystagmus: Its Relation to Visual, Proprioceptive and Vestibular Signals and Cerebellar Atrophy
por: Helmchen, Christoph, et al.
Publicado: (2017)

Hashimoto’s encephalopathy presenting with progressive cerebellar ataxia
por: Al Malik, Yaser M.
Publicado: (2020)

Past, Present and Future Therapeutics for Cerebellar Ataxias
por: Marmolino, D, et al.
Publicado: (2010)

Hashimoto’s Encephalopathy Presenting with Progressive Cerebellar Ataxia
por: Algahtani, Hussein A., et al.
Publicado: (2019)

Gitelman Syndrome Presenting with Cerebellar Ataxia and Tetany
por: Pandya, Shalini, et al.
Publicado: (2023)

Cerebellar atrophy on top of motor neuron compromise as indicator of late-onset GM2 gangliosidosis
por: Hölzer, Hans Thomas, et al.
Publicado: (2021)

Cerebellar pathology in Friedreich's ataxia: Atrophied dentate nuclei with normal iron content
por: Solbach, K., et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_m13tmk12rlc9mctkhn0eai7fab