Brain Calcification and Movement Disorders (Q39093165)

9 September 2017

title

Brain Calcification and Movement Disorders (English)

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9 September 2017

main subject

cerebral calcification

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Vladimir S Kostić

1

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9 September 2017

Igor N Petrović

series ordinal

2

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9 September 2017

publication date

1 January 2017

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Current Neurology and Neuroscience Reports

9 September 2017

published in

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9 September 2017

volume

17

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9 September 2017

issue

1

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9 September 2017

page(s)

2

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Neurological disorders in 166 patients with basal ganglia calcification: a statistical evaluation

9 September 2017

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A rare cause of seizures, parkinsonian, and cerebellar signs: brain calcinosis secondary to thyroidectomy

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Paroxysmal kinesigenic dyskinesia in pseudohypoparathyroidism: is basal ganglia calcification a necessary finding?

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Paroxysmal Nonkinesigenic Dyskinesias Responsive to Carbamazepine in Fahr Syndrome: A Case Report

21 January 2018

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Asymmetric crying facies in the 22q11.2 deletion syndrome: implications for future screening

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Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications

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Extensive intracranial calcifications in a patient with a novel polymerase γ-1 mutation

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Clinicopathological study of diffuse neurofibrillary tangles with calcification. With special reference to TDP-43 proteinopathy and alpha-synucleinopathy

21 January 2018

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Distribution of cerebral cortical lesions in diffuse neurofibrillary tangles with calcification: a clinicopathological study of four autopsy cases showing prominent parietal lobe involvement

21 January 2018

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Atypical occipital calcinosis in a Caucasian individual with probable diffuse neurofibrillary tangles with calcification

21 January 2018

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Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy

21 January 2018

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Leukoencephalopathy, cerebral calcifications and cysts: a family study

21 January 2018

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Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis

21 January 2018

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Bilateral striopallidodentate calcinosis: clinical characteristics of patients seen in a registry

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PDGF, pericytes and the pathogenesis of idiopathic basal ganglia calcification (IBGC).

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Primary familial brain calcification: update on molecular genetics

21 January 2018

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Analysis of gene expression pattern and neuroanatomical correlates for SLC20A2 (PiT-2) shows a molecular network with potential impact in idiopathic basal ganglia calcification ("Fahr's disease").

21 January 2018

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Localization of type-III sodium-dependent phosphate transporter 2 in the mouse brain.

21 January 2018

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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

21 January 2018

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Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification

21 January 2018

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Role of platelet-derived growth factors in physiology and medicine

21 January 2018

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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

21 January 2018

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Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

21 January 2018

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Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia

21 January 2018

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Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers.

21 January 2018

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Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia

21 January 2018

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A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification

21 January 2018

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Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with an SLC20A2 mutation.

21 January 2018

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Novel mutation of SLC20A2 in a Chinese family with primary familial brain calcification

21 January 2018

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Primary familial brain calcification in a Norwegian family, caused by a novel SLC20A2 gene mutation

21 January 2018

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Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB.

21 January 2018

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Progressive brain calcifications and signs in a family with the L9R mutation in the PDGFB gene.

21 January 2018

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Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification

21 January 2018

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Familial idiopathic cerebral calcifications

21 January 2018

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XPR1 mutations are a rare cause of primary familial brain calcification.

21 January 2018

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XPR1: a Gene Linked to Primary Familial Brain Calcification Might Help Explain a Spectrum of Neuropsychiatric Disorders

21 January 2018

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21 January 2018

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Idiopathic basal ganglia calcifications: an atypical presentation of PKAN.

21 January 2018

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Novel PTEN mutation with leukoencephalopathy, basal ganglia calcification and action tremor

21 January 2018

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Basal ganglia calcification in a patient with beta-propeller protein-associated neurodegeneration

21 January 2018

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Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan

21 January 2018

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Intracranial calcification in hyperparathyroidism associated with gait apraxia and parkinsonism

21 January 2018

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21 January 2018

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12 December 2020

A case of MELAS presenting juvenile-onset hyperglycemic chorea-ballism

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study

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12 December 2020

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12 December 2020

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12 December 2020

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome

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12 December 2020

10.1007/S11910-017-0710-9

Identifiers

DOI

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9 September 2017

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