[Polymorphisms of the renin-angiotensin system genes in progressive renal disease]

Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies.

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons·2006

Calculus in a toddler with end-stage renal disease due to prune-belly syndrome.

Oral diseases·2006

Clinical and biochemical manifestations and molecular characterization of the mutation HPRT Jerusalem.

Nucleosides, nucleotides & nucleic acids·2004

The use of Luria's method for the neurobehavioral assessment of encephalopathy in an adolescent: application in a rehabilitation setting.

Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists·2003

Severe reversible renal failure due to naproxen-associated acute interstitial nephritis.

European journal of pediatrics·2001

Familial inheritance of crossed fused renal ectopia.

Pediatric nephrology (Berlin, Germany)·2001

[The Relationship between Physical Activity, Growth, Diagnosis, and Treatment in Children with Attention-Deficit/Hyperactivity Disorder].

Harefuah·2026

[Acute Q Fever in Patients with Risk Factors for a Focalized Persistent Infection - Can Prolonged Antimicrobial Therapy Prevent this Complication?]

Harefuah·2026

[TAVI Program in Centers without an On-Site Cardiac Surgical Department: Outcomes and Feasibility].

Harefuah·2026

[Methadone vs Fentanyl Patch for Prevention of Agitation in Intensive Care Patients: A Before-After Intervention Study].

Harefuah·2026

[Drug Allergies in Elderly Patients: The Outcomes of Allergic Evaluation and Long-Term Follow-up].

Harefuah·2026

[Medical Management Alone in Symptomatic Free-Floating Thrombus of the Carotid Artery].

Harefuah·2026

Identification of Novel Co-Occurring ZNF711 and SRCAP Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.

The application of clinical genetics·2026

Hox/Meis-dependent gene-regulatory transition underlies cardiopharyngeal neural crest diversification.

The EMBO journal·2026

Network analysis of the genetic relationships between twenty psychiatric and substance use disorders.

World psychiatry : official journal of the World Psychiatric Association (WPA)·2026

Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder.

Molecular genetics & genomic medicine·2026

Heterogeneity of azithromycin resistance markers in Neisseria gonorrhoeae and challenges in implementing molecular assays for routine surveillance.

New microbes and new infections·2026

Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.

Biological psychiatry global open science·2026

Related Experiment Videos

[Polymorphisms of the renin-angiotensin system genes in progressive renal disease]

Related Concept Videos

Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodies.

Calculus in a toddler with end-stage renal disease due to prune-belly syndrome.

Clinical and biochemical manifestations and molecular characterization of the mutation HPRT Jerusalem.

The use of Luria's method for the neurobehavioral assessment of encephalopathy in an adolescent: application in a rehabilitation setting.

Severe reversible renal failure due to naproxen-associated acute interstitial nephritis.

Familial inheritance of crossed fused renal ectopia.

[The Relationship between Physical Activity, Growth, Diagnosis, and Treatment in Children with Attention-Deficit/Hyperactivity Disorder].

[Acute Q Fever in Patients with Risk Factors for a Focalized Persistent Infection - Can Prolonged Antimicrobial Therapy Prevent this Complication?]

[TAVI Program in Centers without an On-Site Cardiac Surgical Department: Outcomes and Feasibility].

[Methadone vs Fentanyl Patch for Prevention of Agitation in Intensive Care Patients: A Before-After Intervention Study].

[Drug Allergies in Elderly Patients: The Outcomes of Allergic Evaluation and Long-Term Follow-up].

[Medical Management Alone in Symptomatic Free-Floating Thrombus of the Carotid Artery].

Identification of Novel Co-Occurring ZNF711 and SRCAP Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.

Hox/Meis-dependent gene-regulatory transition underlies cardiopharyngeal neural crest diversification.

Network analysis of the genetic relationships between twenty psychiatric and substance use disorders.

Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder.

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[Polymorphisms of the renin-angiotensin system genes in progressive renal disease]

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