نتایج جستجو برای: caudal dysplasia sequence

تعداد نتایج: 445664  

2016
Dominik P Waluk Gila Zur Ronnie Kaufmann Monika M Welle Vidhya Jagannathan Cord Drögemüller Eliane J Müller Tosso Leeb Arnaud Galichet

X-linked hypohidrotic ectodermal dysplasia (XLHED) caused by variants in the EDA gene represents the most common ectodermal dysplasia in humans. We investigated three male mixed-breed dogs with an ectodermal dysplasia phenotype characterized by marked hypotrichosis and multifocal complete alopecia, almost complete absence of sweat and sebaceous glands, and altered dentition with missing and abn...

Journal: :Philosophical Transactions of the Royal Society B: Biological Sciences 2012

Journal: :razavi international journal of medicine 0
norman ramirez mayaguez medical center, mayaguez, hospital de la concepcion, san german, puerto rico; school of medicine, ponce health sciences university, ponce, puerto rico; mayaguez medical center, mayaguez, hospital de la concepcion, san german, p. o. box: 6847, mayaguez, puerto rico. tel: +1-7872642066 sigfredo villarin school of medicine, ponce health sciences university, ponce, puerto rico robert ritchie ponce research institute, ponce, puerto rico kenira j. thompson department of physiology, neuroscience division, ponce health sciences university, ponce research institute, ponce, puerto rico

conclusions getting a complete knowledge of the condition and evaluating different treatment modalities to treat thoracic insufficiency syndrome. results a direct enlargement of the thorax that will thus provide sufficient space for lung growth; the correction of both the three-dimensional thoracic deformity and the progressive scoliosis. recent findings have revealed that veptr instrumentation...

2017
Sonja Boyd Marko Vannas Kalle Jokelainen Helena Isoniemi Heikki Mäkisalo Martti A Färkkilä Johanna Arola

AIM To investigate markers for high-grade dysplasia for the optimal timing of liver transplantation in patients with primary sclerosing cholangitis (PSC). METHODS Earlier data support a dysplasia-carcinoma sequence, even low- to high-grade dysplasia, in PSC-associated cholangiocarcinoma (CCA). Surveillance using endoscopic retrograde cholangiography (ERC) and brush cytology aims to detect cas...

Journal: :Open Journal of Ophthalmology 2022

Stickler syndrome (SS) is an autosomal dominant inherited genetic disorder that presents with hearing loss, a cleft palate, epiphyseal dysplasia, and degeneration, similar to arthritis well known be associated rhegmato-genous retinal detachments. A particular group of physical features called Pierre Robin sequence also common in people stickler syndrome. includes glossoptosis, micrognathia. We ...

Heidari, A, Tavana, N,

Introduction: Dentin Dysplasia is one of the rare hereditary diseases that the enamel is normal, but it also affects the dentin and  the shape of the tooth pulp. Due to the low prevalence of this disease, a case of dentin dysplasia with the classical and atypical dentin dysplasia type 1 is presented. Case presentation:A 11-year-old girl with the mobility of lower central teeth that has severe ...

2008
UJIHIRO MURAKAMI YOSHIRO KAMEYAMA

INTRODUCTION M A N Y experiments have recently been conducted to investigate the effects of oxygen deficiency upon embryonic development. Embryos offish, amphibia and birds have most frequently been used. Of all these experiments, those of Stockard (1921), of Biichner and his co-workers, and particularly of Rubsaamen (1952), were the most striking. Experiments employing mammals have been very f...

2008
UJIHIRO MURAKAMI YOSHIRO KAMEYAMA

INTRODUCTION M A N Y experiments have recently been conducted to investigate the effects of oxygen deficiency upon embryonic development. Embryos offish, amphibia and birds have most frequently been used. Of all these experiments, those of Stockard (1921), of Biichner and his co-workers, and particularly of Rubsaamen (1952), were the most striking. Experiments employing mammals have been very f...

2011
W. Scott Persons Philip J. Currie

In the South American abelisaurids Carnotaurus sastrei, Aucasaurus garridoi, and, to a lesser extent Skorpiovenator bustingorryi, the anterior caudal ribs project at a high dorsolateral inclination and have interlocking lateral tips. This unique morphology facilitated the expansion of the caudal hypaxial musculature at the expense of the epaxial musculature. Distinct ridges on the ventrolateral...

Journal: :trauma monthly 0
marzieh lak trauma research center, baqiyatallah university of medical sciences, tehran, ir iran; trauma research center, baqiyatallah university of medical sciences tehran, ir iran, tel: +98-9125262585, fax: +98-88053766 hasan araghizadeh trauma research center, baqiyatallah university of medical sciences, tehran, ir iran shahnas shayeghi department of anesthesiology, baqiyatallah university of medical sciences, ir iran behroz khatibi trauma research center, baqiyatallah university of medical sciences, tehran, ir iran

background: pain in infancy is a developmental process. due to the underdeveloped pain pathways in the spinal cord, the threshold of stimulation and sensation of pain is low at birth and has potential impacts on increasing the central effects of pain. primary trauma during infancy can cause long term changes in structure and function of pain pathways that continue until adulthood. lack of pain ...

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