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Keith A Choate

Showing results (41-50 of 115) with videos related to

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Journal of the American Academy of Dermatology|July 23, 2016
Cutaneous skeletal hypophosphatemia syndrome (CSHS) is a multilineage somatic mosaic RASopathyYoung H Lim, Diana Ovejero, Kristina M Derrick, et al.
Pediatric Dermatology|December 4, 2020
Hair and skin predict cardiomyopathies: Carvajal and erythrokeratodermia cardiomyopathy syndromesQisi Sun, Lara Wine Lee, E Kevin Hall, et al.
JAMA Dermatology|December 20, 2018
Genotype-Guided Medical Treatment of an Arteriovenous Malformation in a ChildRamrada Lekwuttikarn, Young H Lim, Shehla Admani, et al.
Journal of the American Academy of Dermatology|November 20, 2012
Capillary malformation-arteriovenous malformation syndrome: identification of a family with a novel mutationLynn M Boyden, Charisse M Orme, Richard J Antaya, et al.
American Journal of Human Genetics|May 7, 2016
Somatic Mutations in NEK9 Cause Nevus ComedonicusJonathan L Levinsohn, Jeffrey L Sugarman, , et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2003
WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epitheliaKeith A Choate, Kristopher T Kahle, Frederick H Wilson, et al.
Pediatric Dermatology|May 14, 2013
Capillary malformation--arteriovenous malformation syndrome: review of the literature, proposed diagnostic criteria, and recommendations for managementCharisse M Orme, Lynn M Boyden, Keith A Choate, et al.
The Journal of Investigative Dermatology|June 11, 2016
Keratoacanthoma Shares Driver Mutations with Cutaneous Squamous Cell CarcinomaYoung H Lim, Jonathan M Fisher, Marcus W Bosenberg, et al.
Pediatric Dermatology|December 24, 2016
Palmoplantar Keratoderma in Costello Syndrome Responsive to AcitretinNareh V Marukian, Jonathan L Levinsohn, Brittany G Craiglow, et al.
The British Journal of Dermatology|May 30, 2025
Linear epidermal naevus associated with a novel mosaic heterozygous PTPN11 variantXingyuan Jiang, Tiffany X Chen, Ronghua Hu, et al.
Pageof 12

Showing results (41-50 of 115) with videos related to

Sort By:
Pageof 12
Journal of the American Academy of Dermatology|July 23, 2016
Cutaneous skeletal hypophosphatemia syndrome (CSHS) is a multilineage somatic mosaic RASopathyYoung H Lim, Diana Ovejero, Kristina M Derrick, et al.
Pediatric Dermatology|December 4, 2020
Hair and skin predict cardiomyopathies: Carvajal and erythrokeratodermia cardiomyopathy syndromesQisi Sun, Lara Wine Lee, E Kevin Hall, et al.
JAMA Dermatology|December 20, 2018
Genotype-Guided Medical Treatment of an Arteriovenous Malformation in a ChildRamrada Lekwuttikarn, Young H Lim, Shehla Admani, et al.
Journal of the American Academy of Dermatology|November 20, 2012
Capillary malformation-arteriovenous malformation syndrome: identification of a family with a novel mutationLynn M Boyden, Charisse M Orme, Richard J Antaya, et al.
American Journal of Human Genetics|May 7, 2016
Somatic Mutations in NEK9 Cause Nevus ComedonicusJonathan L Levinsohn, Jeffrey L Sugarman, , et al.
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2003
WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epitheliaKeith A Choate, Kristopher T Kahle, Frederick H Wilson, et al.
Pediatric Dermatology|May 14, 2013
Capillary malformation--arteriovenous malformation syndrome: review of the literature, proposed diagnostic criteria, and recommendations for managementCharisse M Orme, Lynn M Boyden, Keith A Choate, et al.
The Journal of Investigative Dermatology|June 11, 2016
Keratoacanthoma Shares Driver Mutations with Cutaneous Squamous Cell CarcinomaYoung H Lim, Jonathan M Fisher, Marcus W Bosenberg, et al.
Pediatric Dermatology|December 24, 2016
Palmoplantar Keratoderma in Costello Syndrome Responsive to AcitretinNareh V Marukian, Jonathan L Levinsohn, Brittany G Craiglow, et al.
The British Journal of Dermatology|May 30, 2025
Linear epidermal naevus associated with a novel mosaic heterozygous PTPN11 variantXingyuan Jiang, Tiffany X Chen, Ronghua Hu, et al.
Pageof 12