[Editorial: Vaginal-cytological screening for cervix cancer]

A healthy individual with a homozygous PTCH2 frameshift variant: Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?

Human genome variation·2019

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases.

Journal of inherited metabolic disease·2012

Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy.

Journal of medical genetics·2010

The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein.

Journal of medical genetics·2010

Identification of a novel locus for a USH3 like syndrome combined with congenital cataract.

Clinical genetics·2010

Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency.

Journal of inherited metabolic disease·2009

[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

Interobserver variation among cytopathologists in the evaluation of oncocytic cell-predominant thyroid FNA cytology: A validation study of 173 cases with surgical follow-up and correlation with molecular testing.

Cancer cytopathology·2026

Multidisciplinary Team Care for Early-Stage Lung Cancer in Low- and Middle-Income Countries and Emerging Economies: Current Position and Call for Action.

Thoracic cancer·2026

Neoplastic findings after positive multi-target stool DNA testing in a large gastroenterology practice.

Current medical research and opinion·2026

Multi-scale parallel perception and adaptive feature fusion for chest x-ray multi-disease detection.

Physics in medicine and biology·2026

Brain alterations detected by multiplex magnetic resonance imaging in nasopharyngeal carcinoma patients after induction chemotherapy: a longitudinal study.

PeerJ·2026

When Imaging and Biopsy Mislead: Recurrent Triple-Negative Breast Cancer Mimicking Fat Necrosis.

Cureus·2026

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[Editorial: Vaginal-cytological screening for cervix cancer]

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A healthy individual with a homozygous PTCH2 frameshift variant: Are variants of PTCH2 associated with nevoid basal cell carcinoma syndrome?

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases.

Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy.

The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein.

Identification of a novel locus for a USH3 like syndrome combined with congenital cataract.

Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency.

[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].

Interobserver variation among cytopathologists in the evaluation of oncocytic cell-predominant thyroid FNA cytology: A validation study of 173 cases with surgical follow-up and correlation with molecular testing.

Multidisciplinary Team Care for Early-Stage Lung Cancer in Low- and Middle-Income Countries and Emerging Economies: Current Position and Call for Action.

Neoplastic findings after positive multi-target stool DNA testing in a large gastroenterology practice.

Multi-scale parallel perception and adaptive feature fusion for chest x-ray multi-disease detection.

Brain alterations detected by multiplex magnetic resonance imaging in nasopharyngeal carcinoma patients after induction chemotherapy: a longitudinal study.

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