Results 101 to 110 of about 2,522,601 (164)

Heterogeneity of clinical features and mutation analysis of NTRK1 in Han Chinese patients with congenital insensitivity to pain with anhidrosis

, 2019
Ningbo Li,1 Shanna Guo,1 Qingli Wang,2 Guangyou Duan,3 Jiaoli Sun,1 Yi Liu,1 Jin Zhang,1 Cong Wang,1 Changmao Zhu,1 Jingyu Liu,4 Xianwei Zhang1 1Department of Anesthesiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and ...
Liu Y, Liu J, Wang Q, Zhang J, Wang C, Zhang X, Guo S, Duan G, Sun J, Li N, Zhu C   +10 more
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Poor outcome in congenital mesoblastic nephroma with TPM3::NTRK1 fusion: a case report from multi-disciplinary treatment to molecular tumor board [PDF]

Background: Congenital mesoblastic nephroma (CMN) is a rare renal tumor with good prognosis in children; however, cellular CMN is a special subtype with poor prognosis.
Sun, Mengjiao, Chen, Ji, Deng, Yongji, Hiemcke-Jiwa, Laura S., Fang, Yongjun, Wu, Peng, Xue, Yao, Van Mater, David   +7 more
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Congenital Insensitivity to Pain and Anhidrosis With Orthopedic and Self‐Injury Complications in a 5‐Year‐Old Boy: A Case Report

Clinical Case Reports
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder because of NTRK1 gene mutations, leading to an inability to perceive pain and temperature and lack of sweating. Its rarity and unique clinical challenges, such
Zubair Amin, Humza Saeed, Syed Imam Naufil, Sadaf Saba, Abdullah Imtiaz, Syed Hassan Akhlaq, Muhammad Husnain Ahmad, Masab Ali   +7 more
doaj   +1 more source

Unidirectional Crosstalk Between NTRK1 and IGF2 Drives ER Stress in Chronic Pain

Background: Chronic postsurgical pain (CPSP) poses a major clinical challenge due to unresolved links between neurotrophic pathways and endoplasmic reticulum (ER) stress.
Caixia Zhang, Mi Zhang, Zhang, Xianwei, Zhang, Mi, Bo Jiao, Shangchen Yu, Jiao, Bo, Cao, Xueqin, Yu, Shangchen, Zhang, Kaiwen, Wencui Zhang, Zhang, Caixia, Xueqin Cao, Zhang, Wencui, Xianwei Zhang, Kaiwen Zhang   +15 more
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Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population

, 2008
Hereditary sensory and autonomic neuropathy type IV (HSAN IV), or congenital insensitivity to pain with anhidrosis, is an autosomal recessive disorder characterized by insensitivity to noxious stimuli, anhidrosis from deinnervated sweat glands, and ...
Kaya Bilguvar, Baris Korkmaz, Metin Sabanci, C E Mason, Kemik Hastanesi, R P Lifton, M W State, Elif Ozdamar, B Korkmaz, Aysegul Bursali, M Gunel, K Bilguvar, Beyhan Tüysüz, Fatih Bayrakli, A K Ozturk, Yasar Bayri, B Tüysüz, Y Bayri, C Yalcinkaya, M L Diluna, A Bursali Baltalimani, F Bayrakli, Ali K Ozturk, Richard P Lifton, : M Gunel, Matthew W State, Murat Gunel, Michael L Diluna, E Ozdamar, Cengiz Yalcinkaya, Christopher E Mason   +30 more
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Gene Allen Oral History (part 1)

Gene Allen, Art Director of "My Fair Lady", "A Star is Born", and "Les Girls".

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NTRK1 Gene Fusions Are Frequent in Juvenile Xanthogranuloma. [PDF]

Am J Surg Pathol
Schlögl E, Hürner-Unterberger H, Simonitsch-Klupp I, Amann G, Blank-Foltin J, Neudert B, Wozelka-Oltjan L, Haberler C, Ebetsberger-Dachs G, Müllauer L, Müllauer L.   +10 more
europepmc   +1 more source

Larotrectinib Treatment of Xanthogranuloma With NTRK1 Gene Fusion: A Case Report. [PDF]

Cureus
Ralston G, Humeniuk M.
europepmc   +1 more source

Gene Allen Oral History (part 2)

Gene Allen, Art Director of "My Fair Lady", "A Star is Born", and "Les Girls".

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