نتایج جستجو برای: زبان کوچک دوشاخه bifid uvula

تعداد نتایج: 48100  

2003
Christopher Dean

A method of estimating trunk and branch volumes of single trees is presented that uses a combination of elementary fi eld measurements, terrestrial photography, image rectifi cation and on-screen digitising using commercial software packages and automated volume calculation. The method is applicable to a variety of different sized trees in situations where the trunks are clearly visible. Result...

2014
Ju-Han Kang Kook-Sun Lee Min-Gyu Oh Hwa-Young Choi Sae-Rom Lee Song-Hee Oh Yoon-Joo Choi Gyu-Tae Kim Yong-Suk Choi Eui-Hwan Hwang

PURPOSE This study was performed to investigate the incidence and configuration of the bifid mandibular canal in a Korean population by using cone-beam computed tomography (CBCT) imaging. MATERIALS AND METHODS CBCT images of 1933 patients (884 male and 1049 female) were evaluated using PSR-9000N and Alphard-Vega 3030 Dental CT units (Asahi Roentgen Ind. Co., Ltd, Kyoto, Japan). Image analysis...

Journal: :Internal Medicine 2017

Journal: :The New England journal of medicine 2014
Laura C Tegtmeyer Stephan Rust Monique van Scherpenzeel Bobby G Ng Marie-Estelle Losfeld Sharita Timal Kimiyo Raymond Ping He Mie Ichikawa Joris Veltman Karin Huijben Yoon S Shin Vandana Sharma Maciej Adamowicz Martin Lammens Janine Reunert Anika Witten Esther Schrapers Gert Matthijs Jaak Jaeken Daisy Rymen Tanya Stojkovic Pascal Laforêt François Petit Olivier Aumaître Elzbieta Czarnowska Monique Piraud Teodor Podskarbi Charles A Stanley Reuben Matalon Patricie Burda Soraya Seyyedi Volker Debus Piotr Socha Jolanta Sykut-Cegielska Francjan van Spronsen Linda de Meirleir Pietro Vajro Terry DeClue Can Ficicioglu Yoshinao Wada Ron A Wevers Dieter Vanderschaeghe Nico Callewaert Ralph Fingerhut Emile van Schaftingen Hudson H Freeze Eva Morava Dirk J Lefeber Thorsten Marquardt

BACKGROUND Congenital disorders of glycosylation are genetic syndromes that result in impaired glycoprotein production. We evaluated patients who had a novel recessive disorder of glycosylation, with a range of clinical manifestations that included hepatopathy, bifid uvula, malignant hyperthermia, hypogonadotropic hypogonadism, growth retardation, hypoglycemia, myopathy, dilated cardiomyopathy,...

2017
Dhanashree Sharika Rajashekharan Balamurugan Krishnaswamy Rajagopal Kammara

Although the genus Bifidobacterium was originally named for its bifid morphology, not all bifidobacterial species have a similar structure, and very few of them adopt a bifid shape under stress conditions. The exposure of respective bifidobacterial species to various conditions, such as different pH, temperatures, medium components, in vivo growth in Caenorhabditis elegans, and subculture, did ...

2017
Andrea Andrea Gabrielle Tardieu Christian Fisahn Joe Iwanaga Rod J. Oskouian R. Shane Tubbs

Bifid or bifurcated ribs are a rare anatomical anomaly that accounts for approximately 28% of known rib abnormalities. Bifurcation always occurs at the sternal end of the rib and its two extremities are joined to a bifid costal cartilage. The presence of bifid rib is frequently accompanied by other anomalies, although this does not necessarily imply that it cannot occur as an isolated anomaly. ...

Journal: :Respiratory care 2011
Lily Kristine F Sunio Tahmeed A Contractor Gina Chacon

Bronchoscopy can cause post-procedural throat discomfort due to oropharyngeal irritation. We report a rare complication of bronchoscopy that resulted in similar symptoms. A 30-year-old man complained of severe throat discomfort a day after bronchoscopy. Examination revealed a swollen, elongated uvula. The lower half of the uvula was completely white, consistent with uvular necrosis. He was mana...

2016
Hiroyuki Odagiri Toshiro Iizuka Daisuke Kikuchi Mitsuru Kaise Hidehiko Takeda Kenichi Ohashi Hideo Yasunaga

Previous studies reported that endoscopic resection is effective for the treatment of superficial pharyngeal cancers, as for digestive tract cancers. However, the optimal treatment for superficial cancer of the uvula has not been established because of the rarity of this condition. We present two male patients in their 70s with superficial cancer of the uvula, detected with upper gastrointestin...

Journal: :American journal of medical genetics. Part A 2009
Wuyan Chen Mimi S Kim Sujata Shanbhag Andrew Arai Carol VanRyzin Nazli B McDonnell Deborah P Merke

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is an autosomal recessive disorder and is the most common cause of ambiguous genitalia in the newborn. The genes encoding 21-hydroxylase, CYP21A2, and tenascin-X (TNX), TNXB, are located within the HLA complex, in a region of high gene density termed the RCCX module. The module has multiple pseudogenes as well as tandem repea...

2014
Meltem Ozdemir-Karatas Didem Ozdemir-Ozenen P Suzanne Hart Thomas C Hart

Background. The orofaciodigital syndromes (OFDS) are a heterogeneous group of syndromes that affect the face, oral cavity, and the digits. OFDS type IV (OMIM %258860) is rare and characterized by broad nasal root and tip, orbital hypertelorism or telecanthus, micrognathia, hypoplastic mandible, and low-set ears. Oral symptoms may include cleft lip, cleft or highly arched palate, bifid uvula, cl...

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