[Autosomal dominant polycystic kidney disease. Early diagnosis using DNA marker analysis]

Maternal and foetal outcomes in pregnant patients with active lupus nephritis.

Lupus·2009

Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV.

Human biology·2001

Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language.

American journal of human genetics·2000

Tracing European founder lineages in the Near Eastern mtDNA pool.

American journal of human genetics·2000

mtDNA variation among Greenland Eskimos: the edge of the Beringian expansion.

American journal of human genetics·2000

A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance.

Neurology·1998

[Endovascular treatment of iliofemoral venous thrombosis].

Ugeskrift for laeger·2026

[Lateral epicondylitis].

Ugeskrift for laeger·2026

[Infiltrating basal cell carcinoma with perineural growth in a 15-year-old].

Ugeskrift for laeger·2026

[Group A streptococcal toxic shock syndrome with influenza A and parapneumonic effusion].

Ugeskrift for laeger·2026

[The significance of frailty in the assessment of polypharmacy and deprescribing].

Ugeskrift for laeger·2026

[Nutrition in the prevention and treatment of frailty in older adults].

Ugeskrift for laeger·2026

Expanding the diagnostic lens: Whole exome sequencing in a neonate with arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

Journal of neonatal-perinatal medicine·2026

Severe Transfusion-Dependent Infantile Hemolytic Anemia Associated With a Novel Homozygous PKLR Variant of Uncertain Significance (c.1376C>G, p.Ala459Gly) and Coexisting G6PD Deficiency: A Case Report.

Cureus·2026

Stage-specific neutrophil states in neonatal injury: from antimicrobial deficiency to pro-resolution repair.

Frontiers in immunology·2026

Glycosylated Fibronectin in Fetal Growth Restriction: An Emerging Biomarker of Placental Dysfunction.

Cureus·2026

Palatoglossal Synechia in a Neonate Causing Severe Feeding Problems and Respiratory Distress: First Case Report from Somalia.

Pediatric health, medicine and therapeutics·2026

Idiopathic Epididymo-Orchitis and Pyocele in a Preterm Newborn: A Case Report.

Case reports in pediatrics·2026

Related Experiment Videos

[Autosomal dominant polycystic kidney disease. Early diagnosis using DNA marker analysis]

Related Concept Videos

Maternal and foetal outcomes in pregnant patients with active lupus nephritis.

Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV.

Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language.

Tracing European founder lineages in the Near Eastern mtDNA pool.

mtDNA variation among Greenland Eskimos: the edge of the Beringian expansion.

A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance.

[Endovascular treatment of iliofemoral venous thrombosis].

[Lateral epicondylitis].

[Infiltrating basal cell carcinoma with perineural growth in a 15-year-old].

[Group A streptococcal toxic shock syndrome with influenza A and parapneumonic effusion].

[The significance of frailty in the assessment of polypharmacy and deprescribing].

[Nutrition in the prevention and treatment of frailty in older adults].

Expanding the diagnostic lens: Whole exome sequencing in a neonate with arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

Severe Transfusion-Dependent Infantile Hemolytic Anemia Associated With a Novel Homozygous PKLR Variant of Uncertain Significance (c.1376C>G, p.Ala459Gly) and Coexisting G6PD Deficiency: A Case Report.

Stage-specific neutrophil states in neonatal injury: from antimicrobial deficiency to pro-resolution repair.

Glycosylated Fibronectin in Fetal Growth Restriction: An Emerging Biomarker of Placental Dysfunction.

Palatoglossal Synechia in a Neonate Causing Severe Feeding Problems and Respiratory Distress: First Case Report from Somalia.

Idiopathic Epididymo-Orchitis and Pyocele in a Preterm Newborn: A Case Report.

Related Experiment Videos

[Autosomal dominant polycystic kidney disease. Early diagnosis using DNA marker analysis]

Related Concept Videos

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