Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fadlullah Ba'th"'
Autor:
Rolando R. Rosas, Kristine M. Nachbor, Nathan Handley, Grant Mathison, Beverly R. Wuertz, Fadlullah Ba'th, Frank G. Ondrey
Publikováno v:
Head & Neck. 44:661-671
Head and neck squamous cell carcinoma (HNSCC) requires new treatments and targeted approaches to improve survival. The peroxisome proliferator-activated receptor γ (PPARγ) and retinoic X receptor alpha (RXRα) nuclear receptor pathways may be targe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf1198fd5ccbdbb1c1e935536e855d0
https://doi.org/10.1002/hed.26959
https://doi.org/10.1002/hed.26959
Publikováno v:
The Cleft Palate-Craniofacial Journal. 59:970-975
Objectives: Stickler syndrome (SS) is a heterogeneous inherited connective tissue disorder, often due to a mutation in COL2A1 or COL11A1. Mutations in these genes cause collagen abnormalities affecting ocular, auditory, orofacial, and skeletal system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5e7e0f0dd5ce2b31c2cb1c4f1caf454
https://doi.org/10.1177/10556656211029519
https://doi.org/10.1177/10556656211029519
Publikováno v:
The Cleft Palate-Craniofacial Journal. :105566562211406
Objective Stickler Syndrome (SS) is an inherited collagenopathy characterized by heterogenous orofacial, ocular, auditory, and skeletal abnormalities. The orofacial manifestations are variable and some patients present with cleft palate and velophary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92150e569b2d6a736fff82dc3cb7ff33
https://doi.org/10.1177/10556656221140675
https://doi.org/10.1177/10556656221140675
Publikováno v:
Ear, nose,throat journal.
Prostate cancer is the third most leading cause of cancer in men in the United States. Although expected metastatic spread to bone, liver, and lymph nodes are often monitored, there are other rare presentations that can occur. This case report demons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f7a0eeeff90a347ab10e9d54e9d1966
https://pubmed.ncbi.nlm.nih.gov/34039052
https://pubmed.ncbi.nlm.nih.gov/34039052
Publikováno v:
International journal of pediatric otorhinolaryngology. 146
Objective To determine whether the two most common genetic mutations seen in Stickler Syndrome (SS) (COL2A1 and COL11A1) affect the incidence of mandibular distraction osteogenesis (MDO) and what impact Robin sequence (RS) has on diagnosis. SS is an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::519a73efb12131b919350b75d7050a8a
https://pubmed.ncbi.nlm.nih.gov/34004386
https://pubmed.ncbi.nlm.nih.gov/34004386