S. Moore

The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome

S. Mansour, G. Brice, R. Nagaraja, 2015, European Journal of Human Genetics.

EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis.

Takako Sasaki, S. Ellard, Stacey L. Cole, 2022, American journal of human genetics.

Correlation of the nerve excitability test and electroneurography in acute facial paralysis.

N. J. Coker, S. Moore, J. Fordice, 1992, The American journal of otology.

Suprascapular Nerve Entrapment Secondary to a Lipoma

E. Flatow, S. Miller, M. Hausman, 2003, Clinical orthopaedics and related research.

Hereditary spastic paraparesis presenting as cerebral palsy due to ADD3 variant with mechanistic insight provided by a Drosophila γ‐adducin model

S. Ellard, Edgar Buhl, K. Stals, 2022, Clinical genetics.

Multisequence-imaging protocols to detect cortical lesions of patients with multiple sclerosis: Observations from a post-mortem 3 Tesla imaging study

H. Merkle, B. Yao, H. McFarland, 2009, Journal of the Neurological Sciences.

Postural sensitivity to visual flow in aging adults with and without balance problems.

J. Jensen, M. Woollacott, L. Sundermier, 1996, The journals of gerontology. Series A, Biological sciences and medical sciences.

Expanding the phenotypic spectrum of ALDH18A1-related autosomal recessive cutis laxa with a description of novel neuroradiological findings.

J. Baptista, A. Chakrapani, B. Callewaert, 2021, Clinical dysmorphology.