Taurodontism in X-chromosome aneuploid syndromes

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Work-specific cognitive symptoms and the role of work characteristics, fatigue, and depressive symptoms in cancer patients during 18 months post return to work.

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Fatigue and depressive symptoms improve but remain negatively related to work functioning over 18 months after return to work in cancer patients.

Journal of cancer survivorship : research and practice·2018

X-ray bang-time and fusion reaction history at picosecond resolution using RadOptic detection.

The Review of scientific instruments·2012

High-resolution spectroscopy for Doppler-broadening ion temperature measurements of implosions at the National Ignition Facility.

The Review of scientific instruments·2012

Impact of wind turbine sound on annoyance, self-reported sleep disturbance and psychological distress.

The Science of the total environment·2012

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Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

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Clinical pharmacology and therapeutics·2026

Dynamic risk stratification using early CAR-T expansion in R/R LBCL treated with axicabtagene ciloleucel.

British journal of haematology·2026

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Taurodontism in X-chromosome aneuploid syndromes

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Solid-state framing camera operating in interferometric mode.

Work-specific cognitive symptoms and the role of work characteristics, fatigue, and depressive symptoms in cancer patients during 18 months post return to work.

Fatigue and depressive symptoms improve but remain negatively related to work functioning over 18 months after return to work in cancer patients.

X-ray bang-time and fusion reaction history at picosecond resolution using RadOptic detection.

High-resolution spectroscopy for Doppler-broadening ion temperature measurements of implosions at the National Ignition Facility.

Impact of wind turbine sound on annoyance, self-reported sleep disturbance and psychological distress.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

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Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

S100 Calcium-Binding Protein 16 (S100A16) Promotes Hepatic Stellate Cell Activation Via Erb-B2 Receptor Tyrosine Kinase 2 (ERBB2)-mediated Glycolysis to Facilitate Liver Fibrosis.

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A Rare t(1;11)(q42;q23) Rearrangement with Trisomy 8 and Trisomy 21 in a Pediatric Acute Myeloid Leukemia Patient with Aberrant CD7 Expression and Jacob Syndrome: Diagnostic Value of Conventional Cytogenetics and Fluorescence in Situ Hybridization in a Rapidly Fatal Case.

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Taurodontism in X-chromosome aneuploid syndromes

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