[Hirschsprung's disease: and then three loci]

Expression evaluated by digital image analysis techniques of PRAME more than MCM6 is associated with poor prognosis in neuroblastoma: A pilot study with 84 cases.

Human pathology·2025

Soluble CD89 is a critical factor for mesangial proliferation in childhood IgA nephropathy.

Kidney international·2021

Is magnetic resonance imaging reliable for assessing osteosarcoma of the knee joint in children?

Orthopaedics & traumatology, surgery & research : OTSR·2021

Adrenal ganglioneuromas: a retrospective multicentric study of 104 cases from the COMETE network.

European journal of endocrinology·2021

A variant of ASIC2 mediates sodium retention in nephrotic syndrome.

JCI insight·2021

Rare Collagenous Heterozygote Variants in Children With IgA Nephropathy.

Kidney international reports·2021

[Treatment of chronic hepatitis B: adherence and safety].

Gastroenterologie clinique et biologique·2010

[Long-term therapy for chronic hepatitis B in HIV co-infected patients].

Gastroenterologie clinique et biologique·2010

[Analogs combination therapy in chronic hepatitis B: when and how?].

Gastroenterologie clinique et biologique·2010

[HBsAg seroclearance: prognostic value for the response to treatment and the long-term outcome].

Gastroenterologie clinique et biologique·2010

[HBsAg quantification: virological significance].

Gastroenterologie clinique et biologique·2010

[Influence of treatment on long-term evolution of chronic hepatitis B].

Gastroenterologie clinique et biologique·2010

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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[Hirschsprung's disease: and then three loci]

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Expression evaluated by digital image analysis techniques of PRAME more than MCM6 is associated with poor prognosis in neuroblastoma: A pilot study with 84 cases.

Soluble CD89 is a critical factor for mesangial proliferation in childhood IgA nephropathy.

Is magnetic resonance imaging reliable for assessing osteosarcoma of the knee joint in children?

Adrenal ganglioneuromas: a retrospective multicentric study of 104 cases from the COMETE network.

A variant of ASIC2 mediates sodium retention in nephrotic syndrome.

Rare Collagenous Heterozygote Variants in Children With IgA Nephropathy.

[Treatment of chronic hepatitis B: adherence and safety].

[Long-term therapy for chronic hepatitis B in HIV co-infected patients].

[Analogs combination therapy in chronic hepatitis B: when and how?].

[HBsAg seroclearance: prognostic value for the response to treatment and the long-term outcome].

[HBsAg quantification: virological significance].

[Influence of treatment on long-term evolution of chronic hepatitis B].

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.

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