[Diffuse glioblastosis in children. Clinical and pathologic-anatomical study]

The Regulatory Role of the Oral Commensal Streptococcus mitis on Human Monocytes.

Scandinavian journal of immunology·2017

Capsule expression in Streptococcus mitis modulates interaction with oral keratinocytes and alters susceptibility to human antimicrobial peptides.

Molecular oral microbiology·2015

The short form of TSLP is constitutively translated in human keratinocytes and has characteristics of an antimicrobial peptide.

Mucosal immunology·2014

Polymorphisms in the interleukin-1 gene locus and chronic periodontitis in patients with atherosclerotic and aortic aneurysmal vascular diseases.

Scandinavian journal of immunology·2014

Trefoil factor family 3 expression in the oral cavity.

European journal of oral sciences·2010

NOD1 gene polymorphisms in relation to aggressive periodontitis.

Innate immunity·2009

Use of the auditory brainstem responses by prematures and newborns infants.

Neuropadiatrie·1980

Influence of phenobarbital on the psychomotor development and behaviour in preschool children with convulsions.

Neuropadiatrie·1980

Subdural effusions in children under two years--clinical and computer-tomographical data.

Neuropadiatrie·1980

[Cranial computerized tomography of neonatal encephalopathies. Initial and follow-up studies (author's transl)].

Neuropadiatrie·1980

Congenital muscular dystrophy and cerebral dysgenesis in a Dutch family.

Neuropadiatrie·1980

Sanfilippo A disease in the fetus--comparison with pre- and postnatal cases.

Neuropadiatrie·1980

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

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[Diffuse glioblastosis in children. Clinical and pathologic-anatomical study]

Related Concept Videos

The Regulatory Role of the Oral Commensal Streptococcus mitis on Human Monocytes.

Capsule expression in Streptococcus mitis modulates interaction with oral keratinocytes and alters susceptibility to human antimicrobial peptides.

The short form of TSLP is constitutively translated in human keratinocytes and has characteristics of an antimicrobial peptide.

Polymorphisms in the interleukin-1 gene locus and chronic periodontitis in patients with atherosclerotic and aortic aneurysmal vascular diseases.

Trefoil factor family 3 expression in the oral cavity.

NOD1 gene polymorphisms in relation to aggressive periodontitis.

Use of the auditory brainstem responses by prematures and newborns infants.

Influence of phenobarbital on the psychomotor development and behaviour in preschool children with convulsions.

Subdural effusions in children under two years--clinical and computer-tomographical data.

[Cranial computerized tomography of neonatal encephalopathies. Initial and follow-up studies (author's transl)].

Congenital muscular dystrophy and cerebral dysgenesis in a Dutch family.

Sanfilippo A disease in the fetus--comparison with pre- and postnatal cases.

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.

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[Diffuse glioblastosis in children. Clinical and pathologic-anatomical study]

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