Resultados da pesquisa - "The PJs"

Intranasal administration of elastin-like polypeptide for therapeutic delivery to the central nervous system Por McGowan JWD, Shao Q, Vig PJS, Bidwell III GL

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Perinatal Mortality And Pregnancy Wastage In Ten Punjab Villages During 1991-1996 - A Population Based Study Por Sachar R.K, Soni R.K, Singh W.P, Dhot Ramnik, Gill P.J.S, Arora Sona, Singh Hari, Dhiman B

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Gastrointestinal bleeding after endoscopic mucosal resection in a case of Peutz-Jeghers syndrome with hypofibrinogenemia: A case report Por Toshihiko Kakiuchi, Hironobu Takedomi, Takashi Akutagawa, Nanae Tsuruoka, Yasuhisa Sakata, Muneaki Matsuo

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Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk Por Zhiqing Wang, Shu Liu, Siping Liu, Yadong Wang, Junsheng Chen, Baoping Wu

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A novel <it>de novo </it>mutation in the serine-threonine kinase <it>STK11 </it>gene in a Korean patient with Peutz-Jeghers syndrome Por Ki Chang-Seok, Sun Young-Kyu, Kang Jung-Gu, Choi Yoon-Jung, Yoo Jee-Hyoung, Yoo Jong-Ha, Lee Kyung-A, Choi Jong-Rak

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The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome Por Yu-Liang Jiang, Zi-Ye Zhao, Bai-Rong Li, Fu Yang, Jing Li, Xiao-Wei Jin, Hao Wang, En-Da Yu, Shu-Han Sun, Shou-Bin Ning

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A novel mutation in <it>STK11 </it>gene is associated with Peutz-Jeghers Syndrome in Indian patients Por Singh Lalji, Mohankrishna P, Rao G, Reddy D, Thakur Nikita, Chandak Giriraj R

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Angular cheilitis and oral pigmentation as early detection of Peutz-Jeghers syndrome Por Maharani Laillyza Apriasari, Amy Nindia Carabelly

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A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients Por Wang Zhiqing, Chen Yulan, Wu Baoping, Zheng Haoxuan, He Jiman, Jiang Bo

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Giant gastric polyp in peutz-Jeghers syndrome: Report of a case Por Divya Murali, Anjan Kumar Dhua, Vishesh Jain, Veereshwar Bhatnagar, Rohan Malik, Rajni Yadav

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Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case... Por Zi-Ye Zhao, Yu-Liang Jiang, Bai-Rong Li, Fu Yang, Jing Li, Xiao-Wei Jin, Shou-Bin Ning, Shu-Han Sun

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Mutations in <it>STK11 </it>gene in Czech Peutz-Jeghers patients Por Křepelová Anna, Roubalík Jan, Puchmajerová Alena, Vasovčák Peter

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Peutz-Jeghers syndrome in pediatric patients: experience in a tertiary care institution in Mexico Por Rodrigo Ortegón-Gallareta, Rodrigo Vázquez-Frías, Gerardo Blanco-Rodriguez, Alejandra Consuelo-Sánchez, Claudia Jimena Ortiz-Rivera, Juan Rafael Murillo-Eliosa, Alan I. Vicenteño-León, Pedro Valencia-Mayoral

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High prevalence of germline <it>STK11 </it>mutations in Hungarian Peutz-Jeghers Syndrome patients Por Kasler Miklos, Solyom Szilvia, Kovacs Marietta, Papp Janos, Børresen-Dal, Olah Edith

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Beneficial Effect of Paljeong-san Pharmacopuncture Treatment Combined with Peritoneal Injection on Glycerol-Induced Acute Renal Failure in Rabbits Por Chi-Yeon Lim, Min-Ho Kim, Geum-San Lee, Hyung-Woo Kim, Bu-Yeo Kim, Yeo-Choong Yun, Su-In Cho

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A qualitative research on reproductive concerns of the patients with Peutz-Jeghers syndrome Por Mengxia Pan, Beilei Ye, Huajuan Shen, Jiyong Jin, Qiong Zhang

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A bizarre presentation of Peutz - jegher's syndrome in a 2 year old Por Amir Molaei, Hamidreza Alizadeh Otaghvar, Mohammadreza Tarahomi, Daryanaz Shojaei, Leili Mohajerzadeh, Maryam Baghoori, Feizollah Niazi

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When synchronous mucinous metaplasia and neoplasia of the female genital tract and peutz-jeghers syndrome meet: a case report and literature reviews Por Yue Zhou, Xinyi Wang, Yang Li, Weiru Zhang, Xiaoxuan Xu, Yingxin Pang, Peishu Liu

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Peutz-Jeghers syndrome: A circumventable emergency Por Sourav Choudhury, Anupam Das, Priyankar Misra, Udipta Ray, Sujata Sarangi

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A classical case of Peutz-Jeghers syndrome with brief review of literature Por T. Santosh, M.K. Patro, J. Nayak, B. Behera

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