Evidence for a serum-factor secreted by the human thymus

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.

Neurology·2008

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

Neurology·2006

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

Neurology·2006

'Cap myopathy': case report of a family.

Neuromuscular disorders : NMD·2006

Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms.

Neuropediatrics·2004

[Congenital myasthenic syndromes due to mutations in the rapsyn gene].

Revue neurologique·2004

Belzutifan plus lenvatinib versus cabozantinib in patients with previously treated advanced renal cell carcinoma (LITESPARK-011): an open-label, randomised, controlled, phase 3 trial.

Lancet (London, England)·2026

Switch to once-weekly, single-tablet islatravir-lenacapavir from daily standard of care for HIV-1 (ISLEND-2): a multicentre, randomised, open-label, active-controlled, phase 3 non-inferiority trial.

Lancet (London, England)·2026

[177Lu]Lu-PSMA-617 in patients with PSMA-positive metastatic androgen pathway modulator-naive/sensitive prostate cancer (PSMAddition): a phase 3 randomised, controlled trial.

Lancet (London, England)·2026

B7-H3 expression reflects magnetic resonance imaging (MRI)-derived tumour burden and peritumoral brain oedema in adult gliomas: a radiopathological correlation study.

Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina·2026

Healthy ageing: The struggle for maintaining T cells young.

International immunology·2026

Tislelizumab-induced bullous epidermal necrolysis: case reports and pathogenetic insights.

AME case reports·2026

Deciphering immunosuppressive niches by spatial single-cell proteomics: spatial interaction networks and translational opportunities.

Frontiers in immunology·2026

Low Prevalence of Human T-Cell Lymphotropic Virus Type 1 (HTLV-1) in a Hospital Triage Population in Tehran During 2024-2025.

Health science reports·2026

Diagnostic Accuracy of Combined Fine-Needle Aspiration Biopsy and Ultrasonography for Malignancy in Bethesda III-IV Thyroid Nodules.

Journal of clinical medicine·2026

Related Experiment Videos

Evidence for a serum-factor secreted by the human thymus

Related Concept Videos

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

'Cap myopathy': case report of a family.

Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms.

[Congenital myasthenic syndromes due to mutations in the rapsyn gene].

Belzutifan plus lenvatinib versus cabozantinib in patients with previously treated advanced renal cell carcinoma (LITESPARK-011): an open-label, randomised, controlled, phase 3 trial.

Switch to once-weekly, single-tablet islatravir-lenacapavir from daily standard of care for HIV-1 (ISLEND-2): a multicentre, randomised, open-label, active-controlled, phase 3 non-inferiority trial.

[177Lu]Lu-PSMA-617 in patients with PSMA-positive metastatic androgen pathway modulator-naive/sensitive prostate cancer (PSMAddition): a phase 3 randomised, controlled trial.

B7-H3 expression reflects magnetic resonance imaging (MRI)-derived tumour burden and peritumoral brain oedema in adult gliomas: a radiopathological correlation study.

Healthy ageing: The struggle for maintaining T cells young.

Tislelizumab-induced bullous epidermal necrolysis: case reports and pathogenetic insights.

Deciphering immunosuppressive niches by spatial single-cell proteomics: spatial interaction networks and translational opportunities.

Low Prevalence of Human T-Cell Lymphotropic Virus Type 1 (HTLV-1) in a Hospital Triage Population in Tehran During 2024-2025.

Diagnostic Accuracy of Combined Fine-Needle Aspiration Biopsy and Ultrasonography for Malignancy in Bethesda III-IV Thyroid Nodules.

Related Experiment Videos

Evidence for a serum-factor secreted by the human thymus

Related Concept Videos

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