Search Results - "Levinson, KL"

Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema by Ferrell, Robert E, Karkkainen, Marika J, Lawrence, Elizabeth C, Kimak, Mark A, Levinson, Kara L, McTigue, Michele A, Alitalo, Kari, Finegold, David N

“…Primary lymphoedema is a rare, autosomal dominant disorder that leads to a disabling and disfiguring swelling of the extremities and, when untreated, tends to…”
Get full text

Laparoscopic Abdominal Access Using a Modified Left Upper Quadrant Technique in Morbidly Obese Women Undergoing Gynecologic Surgery by Peijnenburg, EAG, Tanner, EJ, Stone, RL, Levinson, KL, Nickles Fader, A

Get full text

Truncating mutations in FOXC2 cause multiple lymphedema syndromes by FINEGOLD, David N, KIMAK, Mark A, LAWRENCE, Elizabeth C, LEVINSON, Kara L, CHERNISKE, Elizabeth M, POBER, Barbara R, DUNLAP, Jean W, FERRELL, Robert E

“…Hereditary lymphedemas are developmental disorders of the lymphatics resulting in edema of the extremities due to altered lymphatic flow. One such disorder,…”
Get full text

Hereditary Lymphedema: Evidence for Linkage and Genetic Heterogeneity by Ferrell, Robert E., Levinson, Kara L., Esman, Judith H., Kimak, Mark A., Lawrence, Elizabeth C., Michael Barmada, M., Finegold, David N.

“…Hereditary or primary lymphedema is a developmental disorder of the lymphatic system which leads to a disabling and disfiguring swelling of the extremities…”
Get full text

Face perception and within-category discrimination in prosopagnosia by Farah, Martha J., Levinson, Karen L., Klein, Karen L.

“…Prosopagnosics are impaired at face recognition, but unimpaired, or relatively less impaired, at common object recognition. It has been suggested that this…”
Get full text

Age of onset in hereditary lymphedema by Levinson, Kara L., Feingold, Eleanor, Ferrell, Robert E., Glover, Thomas W., Traboulsi, Elias I., Finegold, David N.

“…Objective To characterize age of onset patterns and penetrance in hereditary lymphedema, including differences caused by sex and genetic heterogeneity. Study…”
Get full text

Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13 by Vats, Abhay, Nayak, Alice, Ellis, Demetrius, Randhawa, Parmjeet Singh, Finegold, David N., Levinson, Kara L., Ferrell, Robert E.

“…Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13. Familial nephrotic syndrome (NS) has both autosomal dominant and recessive…”
Get full text

Phonological Dyslexia: Loss of a Reading-specific Component of the Cognitive Architecture? by Farah, Martha J.

“…In phonological dyslexia, nonword reading is impaired while the reading of both regular and irregular words is preserved. Many phonological dyslexics are able…”
Get full text