Cargando…

Mania associated with complicated hereditary spastic paraparesis

Hereditary spastic paraparesis (HSP) is an inherited group of neurological disorders with progressive lower limb spasticity. HSP can be clinically grouped into pure and complicated forms. Pure HSP is one without any associated neurological/psychiatric comorbidity. Depression is the most common psych...

Descripción completa

Detalles Bibliográficos
Autores principales:	Nayak, Raghavendra B, Bhogale, Govind S, Patil, Nanasaheb M, Pandurangi, Aditya A
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications 2011
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159362/ https://www.ncbi.nlm.nih.gov/pubmed/21897689 http://dx.doi.org/10.4103/0976-3147.83592

Ejemplares similares

Clonazepam in the treatment of essential palatal tremors
por: Pandurangi, Aditya A., et al.
Publicado: (2012)

Psychosis in Patients with Systemic Lupus Erythematosus
por: Nayak, Raghavendra B., et al.
Publicado: (2012)

The Coexistence of Multiple Sclerosis and Hereditary Spastic Paraparesis in a Patient
por: Yazıcı, Işıl, et al.
Publicado: (2013)

Intrathecal Baclofen in Hereditary Spastic Paraparesis
por: Pucks-Faes, Elke, et al.
Publicado: (2019)

Dilemmas in Private Psychiatric Practice
por: Patil, Nanasaheb M., et al.
Publicado: (2011)

Gait Patterns in Patients with Hereditary Spastic Paraparesis
por: Serrao, Mariano, et al.
Publicado: (2016)

Serotonin Syndrome Mimicking Intrathecal Baclofen Withdrawal in a Patient with Hereditary Spastic Paraparesis
por: Goffin, Nicolas, et al.
Publicado: (2020)

Gastrointestinal and urinary complaints in adults with hereditary spastic paraparesis
por: Kanavin, Øivind J., et al.
Publicado: (2018)

A Rare Patient with Hereditary Spastic Paraparesis with Parkinsonism
por: Onder, Halil, et al.
Publicado: (2023)

Spastic Paraparesis Following Cocaine Inhalation
por: Savage, Henry Oluwasefunmi, et al.
Publicado: (2009)

First Episode, Late-Onset Organic Mania During the Convalescence Phase of COVID-19: Case Series and Literature Review
por: Kulkarni, Ranganath R., et al.
Publicado: (2022)

Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene
por: Bhattacharjee, Shakya, et al.
Publicado: (2017)

Biotinidase deficiency: A treatable cause of hereditary spastic paraparesis
por: Radelfahr, Florentine, et al.
Publicado: (2020)

Reversible Spastic Paraparesis
por: Kasinathan, Ananthanarayanan, et al.
Publicado: (2019)

Health survey of adults with hereditary spastic paraparesis compared to population study controls
por: Fjermestad, Krister W., et al.
Publicado: (2016)

Pregnancy complicated by HTLV‐1‐associated myelopathy/tropical spastic paraparesis (HAM/TSP): a case report
por: Mori, Hiroshi, et al.
Publicado: (2021)

Health service experiences among adults with hereditary spastic paraparesis or neurofibromatosis type 1
por: Fjermestad, Krister W., et al.
Publicado: (2020)

Pigmented Villonodular Synovitis of the Thoracic Vertebra Presenting with Progressive Spastic Paraparesis
por: Celiktas, Mustafa, et al.
Publicado: (2013)

Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series
por: Andréasson, Mattias, et al.
Publicado: (2019)

MTHFR Deficiency: A Potentially Treatable Cause of Adult-Onset Hereditary Spastic Paraparesis
por: Sudheer, Pachipala, et al.
Publicado: (2022)

Leukodystrophy-Like Presentation in a Child: A Case of Hereditary Spastic Paraparesis-35
por: Sugumar, Kiruthiga, et al.
Publicado: (2022)

An epidemic of spastic paraparesis of unknown aetiology in Northern Mozambique
por: Taibo, Cátia Luciana Abdulfattáhe, et al.
Publicado: (2017)

Muscle paresis and passive stiffness: Key determinants in limiting function in Hereditary and Sporadic Spastic Paraparesis
por: Marsden, Jon, et al.
Publicado: (2012)

Multimodal MRI Longitudinal Assessment of White and Gray Matter in Different SPG Types of Hereditary Spastic Paraparesis
por: Montanaro, Domenico, et al.
Publicado: (2020)

Episodic spastic paraparesis successfully treated with unaided blood transfusions: a case report
por: Pathirage, Loku Pathirage Manoji Muditha Kumari, et al.
Publicado: (2016)

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis
por: Rydning, Siri L, et al.
Publicado: (2019)

Adrenoleukodystrophy as a Cause of Spastic Paraparesis and Hyperpigmentation
por: Chary, Priyanka Kesavan, et al.
Publicado: (2021)

An unusual case of Weil's syndrome with paraparesis
por: Patil, Virendra C., et al.
Publicado: (2011)

Patterns of spinal cord atrophy in HTLV-1 associated myelopathy/ tropical spastic paraparesis (HAM/TSP)
por: Charlip, Emily, et al.
Publicado: (2015)

Oculodentodigital Dysplasia Presenting as Spastic Paraparesis: The First Genetically Confirmed Korean Case and a Literature Review
por: Park, Kye Won, et al.
Publicado: (2017)

Oculo-dento-digital Dysplasia Presenting as Spastic Paraparesis Which Was Successfully Treated by Intrathecal Baclofen Therapy
por: Shinya, Akiko, et al.
Publicado: (2021)

Probable HTLV-I/II Tropical Spastic Paraparesis Patient from Ethiopia: A Case Report
por: Melka, Dereje, et al.
Publicado: (2022)

INTERFERON BETA-1A TREATMENT IN HTLV-1-ASSOCIATED MYELOPATHY/TROPICAL SPASTIC PARAPARESIS: A CASE REPORT
por: Viana, Graça Maria de Castro, et al.
Publicado: (2014)

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)
por: Matsuura, Eiji, et al.
Publicado: (2015)

Novel Complications with HTLV‐1‐associated Myelopathy/Tropical Spastic Paraparesis: Interstitial Cystitis and Persistent Prostatitis
por: Nomata, Koichiro, et al.
Publicado: (1992)

Familial Clusters of HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis
por: Nozuma, Satoshi, et al.
Publicado: (2014)

Early-Onset HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis
por: Schwalb, Alvaro, et al.
Publicado: (2020)

Balance assessment in HTLV-1 associated myelopathy or tropical spastic paraparesis
por: Patrício, Naiane Araújo, et al.
Publicado: (2020)

Predominant Spastic Paraparesis Associated With the D178N Mutation in PRNP
por: Thams, Sebastian, et al.
Publicado: (2021)

Potential oligogenic disease of mental retardation, short stature, spastic paraparesis, and osteopetrosis
por: Alsemari, Abdulaziz, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_s2fjelckes61k3i8ej3c5s5g66