[Instability of myotonic dystrophy CTG trinucleotide repeat]

Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.

Acta neurologica Scandinavica·2015

Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.

Cerebellum (London, England)·2013

Divalent cations enhance fluoride binding to Streptococcus mutans and Streptococcus sanguinis cells and subsequently inhibit bacterial acid production.

Caries research·2012

Affective communication deficits associated with cerebellar degeneration.

Neurocase·2012

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.

Neurology·2012

Objective home-based gait assessment in spinocerebellar ataxia.

Journal of the neurological sciences·2011

[Tibial nerve somatosensory evoked potentials localize the responsible level in tandem spinal stenosis: a case report].

Rinsho shinkeigaku = Clinical neurology·2026

[Cervical cancer metastasis to the lumbosacral spinal root: a case report].

Rinsho shinkeigaku = Clinical neurology·2026

[Ketogenic diet reintroduction in an adult patient with glucose transporter type 1 deficiency syndrome].

Rinsho shinkeigaku = Clinical neurology·2026

[Practice of obstetric medicine in neurological disorders: towards evidence-based shared decision-making (SDM)].

Rinsho shinkeigaku = Clinical neurology·2026

[Hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome with eclampsia, posterior reversible encephalopathy syndrome (PRES), and severe intracerebral hemorrhage in the early postpartum period: a case report].

Rinsho shinkeigaku = Clinical neurology·2026

[A case of anti-N-methyl-D-aspartate (NMDA) receptor encephalitis presenting with characteristic symptoms such as altered sense of time, visual distortion and hallucinations].

Rinsho shinkeigaku = Clinical neurology·2026

Ctf18-dependent localization of interstitial telomeric sequence to nuclear pore complexes prevents chromosome fragility.

Nucleic acids research·2026

Nuclear compartmentalization at the G1/S transition plays a key role in DNA replication control.

Nature communications·2026

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Animal genetics·2026

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

Kidney360·2026

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

The Journal of cell biology·2026

Related Experiment Videos

[Instability of myotonic dystrophy CTG trinucleotide repeat]

Related Concept Videos

Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.

Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.

Divalent cations enhance fluoride binding to Streptococcus mutans and Streptococcus sanguinis cells and subsequently inhibit bacterial acid production.

Affective communication deficits associated with cerebellar degeneration.

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.

Objective home-based gait assessment in spinocerebellar ataxia.

[Tibial nerve somatosensory evoked potentials localize the responsible level in tandem spinal stenosis: a case report].

[Cervical cancer metastasis to the lumbosacral spinal root: a case report].

[Ketogenic diet reintroduction in an adult patient with glucose transporter type 1 deficiency syndrome].

[Practice of obstetric medicine in neurological disorders: towards evidence-based shared decision-making (SDM)].

[Hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome with eclampsia, posterior reversible encephalopathy syndrome (PRES), and severe intracerebral hemorrhage in the early postpartum period: a case report].

[A case of anti-N-methyl-D-aspartate (NMDA) receptor encephalitis presenting with characteristic symptoms such as altered sense of time, visual distortion and hallucinations].

Ctf18-dependent localization of interstitial telomeric sequence to nuclear pore complexes prevents chromosome fragility.

Nuclear compartmentalization at the G1/S transition plays a key role in DNA replication control.

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Type, Location and Zygosity of KCNJ16 Variants May Determine the Clinical Severity of Hypokalemia Tubulopathy and Deafness (HkTD).

Differential contributions of β-tubulin isotypes to acentrosomal oocyte meiosis in C. elegans.

Related Experiment Videos

[Instability of myotonic dystrophy CTG trinucleotide repeat]

Related Concept Videos

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