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Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic Markers.

JIMD reports·2015

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Clinical genetics·2013

What can we learn from old microdeletion syndromes using array-CGH screening?

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[Digitoxin poisoning: reversing ventricular fibrillation with Fab fragments of anti-digoxin antibody].

La Nouvelle presse medicale·1982

[Treatment of acute myeloid leukemia with a protocol combining intensive induction chemotherapy, early consolidation treatment, splenectomy and long-term maintenance chemotherapy. Preliminary study].

La Nouvelle presse medicale·1982

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La Nouvelle presse medicale·1982

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La Nouvelle presse medicale·1982

Juanbi Tang Attenuates Intervertebral Disc Degeneration by Suppressing p38MAPK/NF-κB Signaling and Activating Atg5-Dependent Autophagy to Promote Macrophage M2 Polarization: In Vivo and In Vitro Evidence.

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Reumatismo·2026

Progressive multifocal leukoencephalopathy during bispecific antibody therapy in multiple myeloma: from immune dysfunction to early recognition. Comment on: "Progressive multifocal leukoencephalopathy and BK virus-nephropathy with bispecific antibody therapy in multiple myeloma".

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Isolated atrial amyloidosis from atrial natriuretic peptide - a common but overlooked cardiac condition.

Upsala journal of medical sciences·2026

Epigenetic reprogramming in autoimmune and immune-mediated skin disease.

Frontiers in immunology·2026

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Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.

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