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Quoted phrase not found in phrase index: "Subcortical white matter calcifications"
Page 1
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
Ashrafi MR, Amanat M, Garshasbi M, Kameli R, Nilipour Y, Heidari M, Rezaei Z, Tavasoli AR. Ashrafi MR, et al. Expert Rev Neurother. 2020 Jan;20(1):65-84. doi: 10.1080/14737175.2020.1699060. Epub 2019 Dec 12. Expert Rev Neurother. 2020. PMID: 31829048 Review.
Introduction: Leukodystrophies constitute heterogenous group of rare heritable disorders primarily affecting the white matter of central nervous system. These conditions are often under-appreciated among physicians. ...Comprehensive evaluation of clinical findings, …
Introduction: Leukodystrophies constitute heterogenous group of rare heritable disorders primarily affecting the white matter …
Fahr's syndrome: literature review of current evidence.
Saleem S, Aslam HM, Anwar M, Anwar S, Saleem M, Saleem A, Rehmani MA. Saleem S, et al. Orphanet J Rare Dis. 2013 Oct 8;8:156. doi: 10.1186/1750-1172-8-156. Orphanet J Rare Dis. 2013. PMID: 24098952 Free PMC article. Review.
Calcified deposits are made up of calcium carbonate and calcium phosphate, and are commonly located in the Basal Ganglia, Thalamus, Hippocampus, Cerebral cortex, Cerebellar Subcortical white matter and Dentate Nucleus. Molecular genetics of this disease haven …
Calcified deposits are made up of calcium carbonate and calcium phosphate, and are commonly located in the Basal Ganglia, Thalamus, Hippocam …
The Genetics of Primary Familial Brain Calcification: A Literature Review.
Chen SY, Ho CJ, Lu YT, Lin CH, Lan MY, Tsai MH. Chen SY, et al. Int J Mol Sci. 2023 Jun 29;24(13):10886. doi: 10.3390/ijms241310886. Int J Mol Sci. 2023. PMID: 37446066 Free PMC article. Review.
Primary familial brain calcification (PFBC), also known as Fahr's disease, is a rare inherited disorder characterized by bilateral calcification in the basal ganglia according to neuroimaging. Other brain regions, such as the thalamus, cerebellum, and subcortical …
Primary familial brain calcification (PFBC), also known as Fahr's disease, is a rare inherited disorder characterized by bilateral …
Clinical and imaging diagnosis for heredodegenerative diseases.
Boddaert N, Brunelle F, Desguerre I. Boddaert N, et al. Handb Clin Neurol. 2013;111:63-78. doi: 10.1016/B978-0-444-52891-9.00006-3. Handb Clin Neurol. 2013. PMID: 23622151 Review.
Anomalies disclosed after 3 months of age include basal ganglia appearing hyper- or hypointense on T2, hypointense on T2*, or calcified white matter anomalies mainly periventricular or subcortical, or with contrast enhancement, associated with macrocephaly an …
Anomalies disclosed after 3 months of age include basal ganglia appearing hyper- or hypointense on T2, hypointense on T2*, or calcified w …
Fahr's disease: A rare neuropsychiatric disorder.
Sipra ZS, Din IU, Awais MA, Tariq TA. Sipra ZS, et al. J Pak Med Assoc. 2022 Feb;72(2):383. doi: 10.47391/JPMA.22-40. J Pak Med Assoc. 2022. PMID: 35320202 Free article.
Fahr's disease is a rare clinical neurodegenerative entity, occurring mainly in 4th or 5th decade, showing gradually progressive bilateral symmetric calcifications in basal ganglia, subcortical white matter, thalami or cerebellum, which can lead to mov …
Fahr's disease is a rare clinical neurodegenerative entity, occurring mainly in 4th or 5th decade, showing gradually progressive bilateral s …
Update on several/certain adult-onset genetic leukoencephalopathies: clinical signs and molecular confirmation.
Di Donato I, Dotti MT, Federico A. Di Donato I, et al. J Alzheimers Dis. 2014;42 Suppl 3:S27-35. doi: 10.3233/JAD-141026. J Alzheimers Dis. 2014. PMID: 24958462 Review.
In particular, we review the clinical spectrum and the molecular pathogenesis of certain adult-onset leukoencephalopathies, including cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), cerebral autosomal recessive arteriop …
In particular, we review the clinical spectrum and the molecular pathogenesis of certain adult-onset leukoencephalopathies, including cerebr …
Inborn errors of metabolism: combining clinical and radiologic clues to solve the mystery.
Ibrahim M, Parmar HA, Hoefling N, Srinivasan A. Ibrahim M, et al. AJR Am J Roentgenol. 2014 Sep;203(3):W315-27. doi: 10.2214/AJR.13.11154. AJR Am J Roentgenol. 2014. PMID: 25148190 Review.
., macrocephaly), geographic distribution of lesions (e.g., subcortical vs deep white matter or frontal vs parietooccipital), and other imaging features (e.g., contrast enhancement, calcification, cysts, and cortical dysplasia). ...
., macrocephaly), geographic distribution of lesions (e.g., subcortical vs deep white matter or frontal vs parietooccip …
Magnetic resonance imaging of anterior temporal lobe cysts in children: discriminating special imaging features in a particular group of diseases.
Nunes RH, Pacheco FT, da Rocha AJ. Nunes RH, et al. Neuroradiology. 2014 Jul;56(7):569-77. doi: 10.1007/s00234-014-1356-9. Epub 2014 Apr 23. Neuroradiology. 2014. PMID: 24756164 Review.
METHODS: A literature search was conducted, and institutional imaging files were reviewed to identify MR examinations with ATL cysts in children. Patients were divided according to head size, calcifications, white matter and cortical abnormalities. Unsupervis …
METHODS: A literature search was conducted, and institutional imaging files were reviewed to identify MR examinations with ATL cysts in chil …
Fahr's syndrome and clinical correlation: a case series and literature review.
Pistacchi M, Gioulis M, Sanson F, Marsala SM. Pistacchi M, et al. Folia Neuropathol. 2016;54(3):282-294. doi: 10.5114/fn.2016.62538. Folia Neuropathol. 2016. PMID: 27764521 Free article. Review.
INTRODUCTION: Fahr's disease is characterized by bilateral calcium deposition within the basal ganglia, cerebellar dentate nucleus and subcortical brain white matter. The main clinical manifestations are rigid or hyperkinetic syndrome, mood disorders and cogn …
INTRODUCTION: Fahr's disease is characterized by bilateral calcium deposition within the basal ganglia, cerebellar dentate nucleus and su …
Congenital Zika syndrome with arthrogryposis: retrospective case series study.
van der Linden V, Filho EL, Lins OG, van der Linden A, Aragão Mde F, Brainer-Lima AM, Cruz DD, Rocha MA, Sobral da Silva PF, Carvalho MD, do Amaral FJ, Gomes JA, Ribeiro de Medeiros IC, Ventura CV, Ramos RC. van der Linden V, et al. BMJ. 2016 Aug 9;354:i3899. doi: 10.1136/bmj.i3899. BMJ. 2016. PMID: 27509902 Free PMC article.
Five of the children underwent brain computed tomography (CT) and magnetic resonance imaging (MRI) and the remaining two CT only. All presented malformations of cortical development, calcifications predominantly in the cortex and subcortical white matter …
Five of the children underwent brain computed tomography (CT) and magnetic resonance imaging (MRI) and the remaining two CT only. All presen …
56 results