[An error of the figures in the article on malignant skin melanomas]

Usefulness of discography, discoblock and a new mechanical method for identifying a painful segment/disc.

Neuro-Chirurgie·2022

Raman spectra of high- κ dielectric layers investigated with micro-Raman spectroscopy comparison with silicon dioxide.

TheScientificWorldJournal·2013

Contractile activity of human skeletal muscle cells prevents insulin resistance by inhibiting pro-inflammatory signalling pathways.

Diabetologia·2012

Cannabinoid type 1 receptors in human skeletal muscle cells participate in the negative crosstalk between fat and muscle.

Diabetologia·2008

Reproducibility of tumor response evaluation in patients with high-grade malignant non-Hodgkin's lymphoma.

Medical oncology (Northwood, London, England)·2002

Risk in numbers--difficulties in the transformation of genetic knowledge from research to people--the case of hereditary cancer.

Acta oncologica (Stockholm, Sweden)·2001

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

Lakartidningen·2026

[Rare manifestations of giant cell arteritis].

Lakartidningen·2026

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

Lakartidningen·2026

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

Lakartidningen·2026

[Postoperative atrial fibrillation after open heart surgery].

Lakartidningen·2026

[Interaction between psychotic patients and AI-driven chatbots].

Lakartidningen·2026

Association of doxycycline treatment with time to first documented MP-RNA negative conversion in pediatric Mycoplasma pneumoniae pneumonia: a retrospective cohort study.

Italian journal of pediatrics·2026

Anatomical location defines distinct molecular subtypes of mucosal melanoma.

ESMO open·2026

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Human molecular genetics·2026

Meissnerian neurofibroma: A rare histological variant of neurofibroma.

Indian journal of pathology & microbiology·2026

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

The Journal of experimental medicine·2026

Acidic Stress Induces Proteomic Reprogramming and Virulence-Associated Adaptation in Paracoccidioides brasiliensis.

Journal of proteome research·2026

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[An error of the figures in the article on malignant skin melanomas]

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Usefulness of discography, discoblock and a new mechanical method for identifying a painful segment/disc.

Raman spectra of high- κ dielectric layers investigated with micro-Raman spectroscopy comparison with silicon dioxide.

Contractile activity of human skeletal muscle cells prevents insulin resistance by inhibiting pro-inflammatory signalling pathways.

Cannabinoid type 1 receptors in human skeletal muscle cells participate in the negative crosstalk between fat and muscle.

Reproducibility of tumor response evaluation in patients with high-grade malignant non-Hodgkin's lymphoma.

Risk in numbers--difficulties in the transformation of genetic knowledge from research to people--the case of hereditary cancer.

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

[Rare manifestations of giant cell arteritis].

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

[Postoperative atrial fibrillation after open heart surgery].

[Interaction between psychotic patients and AI-driven chatbots].

Association of doxycycline treatment with time to first documented MP-RNA negative conversion in pediatric Mycoplasma pneumoniae pneumonia: a retrospective cohort study.

Anatomical location defines distinct molecular subtypes of mucosal melanoma.

Myofibrillar myopathy-associated KY protein promotes muscle fibre size rescue independent of its predicted catalytic triad.

Meissnerian neurofibroma: A rare histological variant of neurofibroma.

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

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