Genetics of immunity deficiency syndromes

Preoperative and intraoperative factors predictive of complications and stricture recurrence following multiple urethroplasty techniques.

BJUI compass·2022

Molecular evidence for shifts in polysaccharide composition associated with adaptation of soybean Bradyrhizobium strains to the Brazilian Cerrado soils.

Environmental microbiology·2001

Using the ICSOoL to measure the impact of lower urinary tract symptoms on quality of life: evidence from the ICS-'BPH' Study. International Continence Society--Benign Prostatic Hyperplasia.

British journal of urology·1997

The International Continence Society "Benign Prostatic Hyperplasia" Study: international differences in lower urinary tract symptoms and related bother.

The Journal of urology·1997

The International Continence Society "Benign Prostatic Hyperplasia" Study: the botherosomeness of urinary symptoms.

The Journal of urology·1997

The ICS-'BPH' Study: the psychometric validity and reliability of the ICSmale questionnaire.

British journal of urology·1996

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

Journal of medical genetics·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Evolving roles within the genomic medicine workforce: a revised framework for UK practice-position on behalf of the Association of Genetic Nurses and Counsellors and the Clinical Genetics Society.

Journal of medical genetics·2026

Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank.

Journal of medical genetics·2026

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

Journal of medical genetics·2026

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

Journal of medical genetics·2026

Development and internal validation of a machine learning-based disease burden index for irritable bowel syndrome: a multicentre cross-sectional study.

Annals of medicine·2026

Epidemiology and Outcome of Early Acute Kidney Injuries in Patients with Acute Intracerebral Hemorrhage Admitted to the Apex Neurosciences Center in Dubai.

Saudi journal of medicine & medical sciences·2026

Distinguishing Acute Myocardial Infarction from Other Forms of Cardiac Injury with the Cardiac Troponin Long-T ITC Complex and High-Sensitivity Troponin I and T in Patients with Suspected Acute Coronary Syndrome: MERITnI Substudy.

Clinical chemistry·2026

Collagenous gastritis: current understanding of a rare immune-mediated gastropathy across pediatric and adult phenotypes-from pathogenesis to therapeutic strategies.

Frontiers in cell and developmental biology·2026

A retrospective analysis of initial ultrasonographic misdiagnosis of fibrous hamartoma of infancy at the ultrasound center of a tertiary hospital in China.

Frontiers in pediatrics·2026

Evolving role of intestinal ultrasound in the evaluation of Crohn's disease: A clinical- radiological perspective.

European journal of radiology open·2026

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Genetics of immunity deficiency syndromes

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Preoperative and intraoperative factors predictive of complications and stricture recurrence following multiple urethroplasty techniques.

Molecular evidence for shifts in polysaccharide composition associated with adaptation of soybean Bradyrhizobium strains to the Brazilian Cerrado soils.

Using the ICSOoL to measure the impact of lower urinary tract symptoms on quality of life: evidence from the ICS-'BPH' Study. International Continence Society--Benign Prostatic Hyperplasia.

The International Continence Society "Benign Prostatic Hyperplasia" Study: international differences in lower urinary tract symptoms and related bother.

The International Continence Society "Benign Prostatic Hyperplasia" Study: the botherosomeness of urinary symptoms.

The ICS-'BPH' Study: the psychometric validity and reliability of the ICSmale questionnaire.

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Evolving roles within the genomic medicine workforce: a revised framework for UK practice-position on behalf of the Association of Genetic Nurses and Counsellors and the Clinical Genetics Society.

Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank.

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

Development and internal validation of a machine learning-based disease burden index for irritable bowel syndrome: a multicentre cross-sectional study.

Epidemiology and Outcome of Early Acute Kidney Injuries in Patients with Acute Intracerebral Hemorrhage Admitted to the Apex Neurosciences Center in Dubai.

Distinguishing Acute Myocardial Infarction from Other Forms of Cardiac Injury with the Cardiac Troponin Long-T ITC Complex and High-Sensitivity Troponin I and T in Patients with Suspected Acute Coronary Syndrome: MERITnI Substudy.

Collagenous gastritis: current understanding of a rare immune-mediated gastropathy across pediatric and adult phenotypes-from pathogenesis to therapeutic strategies.

A retrospective analysis of initial ultrasonographic misdiagnosis of fibrous hamartoma of infancy at the ultrasound center of a tertiary hospital in China.

Evolving role of intestinal ultrasound in the evaluation of Crohn's disease: A clinical- radiological perspective.

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Genetics of immunity deficiency syndromes

Related Concept Videos

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