The genetics of nocturnal enuresis: a simple question of complexity

Survey of unlicensed and off label drug use in paediatric wards in European countries. European Network for Drug Investigation in Children.

BMJ (Clinical research ed.)·2000

Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.

Acta ophthalmologica Scandinavica·1999

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis.

Nature genetics·1998

Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22.

Human genetics·1997

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.

Journal of medical genetics·1997

An echocardiographic study comparing male Swedish elite orienteers with other elite endurance athletes.

The American journal of cardiology·1997

Diagnostic Performance of Recombinant Peanut Allergens in Children: sIgE Cut-Offs and Anaphylaxis Risk.

Acta paediatrica (Oslo, Norway : 1992)·2026

Remote Early Follow-Up: Home Videos Enabled Reliable General Movement Assessment With Only Weak Association With the Ages and Stages Questionnaire.

Acta paediatrica (Oslo, Norway : 1992)·2026

Clinical Application of a Neonatal Delirium Screening Tool: A Feasibility Study.

Acta paediatrica (Oslo, Norway : 1992)·2026

Factors Associated With Omalizumab Response in Chronic Spontaneous Urticaria: Are There Age-Related Differences?

Acta paediatrica (Oslo, Norway : 1992)·2026

Feasibility of Thermal Imaging for Contactless Respiratory Monitoring in Children.

Acta paediatrica (Oslo, Norway : 1992)·2026

Optimising Human Papillomavirus Vaccination Strategies for Faster Cervical Cancer Elimination.

Acta paediatrica (Oslo, Norway : 1992)·2026

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

Related Experiment Videos

The genetics of nocturnal enuresis: a simple question of complexity

Related Concept Videos

Survey of unlicensed and off label drug use in paediatric wards in European countries. European Network for Drug Investigation in Children.

Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis.

Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22.

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.

An echocardiographic study comparing male Swedish elite orienteers with other elite endurance athletes.

Diagnostic Performance of Recombinant Peanut Allergens in Children: sIgE Cut-Offs and Anaphylaxis Risk.

Remote Early Follow-Up: Home Videos Enabled Reliable General Movement Assessment With Only Weak Association With the Ages and Stages Questionnaire.

Clinical Application of a Neonatal Delirium Screening Tool: A Feasibility Study.

Factors Associated With Omalizumab Response in Chronic Spontaneous Urticaria: Are There Age-Related Differences?

Feasibility of Thermal Imaging for Contactless Respiratory Monitoring in Children.

Optimising Human Papillomavirus Vaccination Strategies for Faster Cervical Cancer Elimination.

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

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The genetics of nocturnal enuresis: a simple question of complexity

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