Some pathogenetic aspects of Borna disease

Extraventricular neurocytoma of the spinal cord in a dog.

Veterinary pathology·2008

Synphilin-1 isoforms in Parkinson's disease: regulation by phosphorylation and ubiquitylation.

Cellular and molecular life sciences : CMLS·2007

Spontaneous and experimental glycoprotein storage disease of goats induced by Ipomoea carnea subsp fistulosa (Convolvulaceae).

Veterinary pathology·2007

Headache associated with sexual activity: demography, clinical features, and comorbidity.

Neurology·2003

Cognitive processing in headache associated with sexual activity.

Cephalalgia : an international journal of headache·2003

Evidence of infectious diseases in harbour porpoises (Phocoena phocoena) hunted in the waters of Greenland and by-caught in the German North Sea and Baltic Sea.

The Veterinary record·2001

Neuroanatomy of dreaming and REM phenomenology.

Progress in brain research·2026

Brain oscillations and sleep microarchitecture: From EEG to fMRI.

Progress in brain research·2026

Sleep, attention, and executive function in health and disease.

Progress in brain research·2026

Sleep, emotional regulation, and limbic-cortical dynamics: From basic mechanisms to clinical translation.

Progress in brain research·2026

Sleep and memory consolidation: Neural and cognitive perspectives.

Progress in brain research·2026

Neural mechanisms and architecture of sleep.

Progress in brain research·2026

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

Related Experiment Videos

Some pathogenetic aspects of Borna disease

Related Concept Videos

Extraventricular neurocytoma of the spinal cord in a dog.

Synphilin-1 isoforms in Parkinson's disease: regulation by phosphorylation and ubiquitylation.

Spontaneous and experimental glycoprotein storage disease of goats induced by Ipomoea carnea subsp fistulosa (Convolvulaceae).

Headache associated with sexual activity: demography, clinical features, and comorbidity.

Cognitive processing in headache associated with sexual activity.

Evidence of infectious diseases in harbour porpoises (Phocoena phocoena) hunted in the waters of Greenland and by-caught in the German North Sea and Baltic Sea.

Neuroanatomy of dreaming and REM phenomenology.

Brain oscillations and sleep microarchitecture: From EEG to fMRI.

Sleep, attention, and executive function in health and disease.

Sleep, emotional regulation, and limbic-cortical dynamics: From basic mechanisms to clinical translation.

Sleep and memory consolidation: Neural and cognitive perspectives.

Neural mechanisms and architecture of sleep.

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Related Experiment Videos

Some pathogenetic aspects of Borna disease

Related Concept Videos

Related Articles