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Your search keyword '"Latham, Lea"' showing total 11 results

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11 results on '"Latham, Lea"'

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1. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

2. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

3. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

4. Correction to:An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

6. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

7. Higher Incidence of Osteonecrosis of the Jaw (ONJ) in Patients with Metastatic Castration Resistant Prostate Cancer Treated with Anti-Angiogenic Agents.

9. Safety, pharmacokinetics and sialic acid production after oral administration of N-acetylmannosamine (ManNAc) to subjects with GNE myopathy.

10. Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation.

11. Phase II trial of bevacizumab, thalidomide, docetaxel, and prednisone in patients with metastatic castration-resistant prostate cancer.

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