Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ramrada Lekwuttikarn"'
Autor:
Pharuhad Pongmee, Sanchawan Wittayakornrerk, Ramrada Lekwuttikarn, Sasikarn Pakdeeto, Piangor Watcharakuldilok, Chatchay Prempunpong, Thipwimol Tim-Aroon, Chawintee Puttanapitak, Piyawan Wattanasoontornsakul, Thitiporn Junhasavasdikul, Parith Wongkittichote, Saisuda Noojarern, Duangrurdee Wattanasirichaigoon
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Epidermolysis bullosa (EB) is a rare and genetically heterogeneous disorder characterized by skin fragility and blister formation occurring spontaneously or after minor trauma. EB is accompanied by congenital absence of skin (EB with CAS) in some pat
Externí odkaz:
https://doaj.org/article/f06f261dd0a940148bd0425b6f476bcd
Autor:
Taehan Kim, Elidia Tafoya, Malcolm P Chelliah, Ramrada Lekwuttikarn, Jiang Li, Kavita Y Sarin, Joyce Teng
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0213872 (2019)
Lymphatic malformation (LM) is a developmental anomaly of the lymphatic system that may lead to disfigurement, organ dysfunction and recurrent infection. Though several treatment modalities exist, pharmacotherapy is often associated with side effects
Externí odkaz:
https://doaj.org/article/d9bbcf8974bd4b408d70725cacae50e7
Publikováno v:
Journal of Cosmetic Dermatology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fbe3cbe5a297c71892f2cdaf000651c
https://doi.org/10.1111/jocd.15727
https://doi.org/10.1111/jocd.15727
Autor:
Elidia Tafoya, Joyce M.C. Teng, Ramrada Lekwuttikarn, Monica Martin, Gun Ho Lee, Kavita Y. Sarin
Publikováno v:
The Journal of investigative dermatology. 142(2)
Expression-based systematic drug repositioning has been explored to predict novel treatments for a number of skin disorders. In this study, we utilize this approach to identify, to our knowledge, previously unreported therapies for epidermolysis bull
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f8e6a4acf41408489a3da99277ad13
https://pubmed.ncbi.nlm.nih.gov/34924185
https://pubmed.ncbi.nlm.nih.gov/34924185
Autor:
Ramrada Lekwuttikarn, Joyce M.C. Teng
Publikováno v:
Current Opinion in Pediatrics. 30:505-513
Childhood malnutrition is a major global health issue. It is often thought of as a developing world problem and therefore, underdiagnosed or misdiagnosed in developed countries. The delay in diagnosis and treatment can lead to increased morbidity and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f801d3b53cfe42fe361707bada81dff
https://doi.org/10.1097/mop.0000000000000652
https://doi.org/10.1097/mop.0000000000000652
Publikováno v:
International Journal of Dermatology. 56:884-888
The high prevalence of acne vulgaris in teenagers has increased comorbidities. Lasers offer alternative options for acne treatment because they have rapid action, low systemic adverse effects, and do not require everyday treatment. To study the effic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19b2559563dfba0a22f300ba07cac283
https://doi.org/10.1111/ijd.13631
https://doi.org/10.1111/ijd.13631
Publikováno v:
Pediatrics. 144
Hepatic hemangioma (HH) is a common asymptomatic, self-limiting benign vascular tumor of the liver in neonates. Although complicated HHs are rare, they have significant risks of morbidity and mortality, especially during the perinatal period. Because
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::664905ac495395afbfc521e0dbd9f5b7
https://doi.org/10.1542/peds.2019-1339
https://doi.org/10.1542/peds.2019-1339
Publikováno v:
Dermatologic Therapy. 32
Maffucci syndrome is a rare genetic disease due to somatic mutation of IDH1 gene. Currently there is no medical treatment available for spindle cell hemangioma associated with this disorder. Here we report successful management of these hemangiomas u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1dfa91974c95e42892b512852597137
https://doi.org/10.1111/dth.12919
https://doi.org/10.1111/dth.12919
Publikováno v:
JAMA dermatology. 155(2)
Importance: Genetic testing results can provide guidance in developing personalized treatment plans for patients with vascular anomalies. Objective: To explore the efficacy of tramitinib in the treatment of an extracranial arteriovenous malformation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5380ef553a9d90cb33f00a5ce45d4eeb
https://pubmed.ncbi.nlm.nih.gov/30566190
https://pubmed.ncbi.nlm.nih.gov/30566190
Autor:
Ramrada Lekwuttikarn, Kavita Y. Sarin, Joyce M.C. Teng, Jiang Li, Elidia Tafoya, Taehan Kim, Malcolm P. Chelliah
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 4, p e0213872 (2019)
PLoS ONE, Vol 14, Iss 4, p e0213872 (2019)
Lymphatic malformation (LM) is a developmental anomaly of the lymphatic system that may lead to disfigurement, organ dysfunction and recurrent infection. Though several treatment modalities exist, pharmacotherapy is often associated with side effects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8844775e7baef056667b19037653853
https://pubmed.ncbi.nlm.nih.gov/30947262
https://pubmed.ncbi.nlm.nih.gov/30947262