نتایج جستجو برای: multiple hereditary

تعداد نتایج: 831640  

2016
Diane Pivot Marc Debouverie Michel Grzebyk David Brassat Michel Clanet Pierre Clavelou Christian Confavreux Gilles Edan Emmanuelle Leray Thibault Moreau Sandra Vukusic Guy Hédelin Francis Guillemin

INTRODUCTION Geographical variation in the prevalence of multiple sclerosis (MS) is controversial. Heterogeneity is important to acknowledge to adapt the provision of care within the healthcare system. We aimed to investigate differences in prevalence of MS in departments in the French territory. METHODS We estimated MS prevalence on October 31, 2004 in 21 administrative departments in France...

Journal: :Journal of medical genetics 1988
R M Winter R D Clark K Ashley G Gibbs

A combinatorial method is described for grouping cases with multiple malformations for the purpose of identifying previously undescribed syndromes. This method includes ways of carrying out 'tight' or 'loose' grouping, of allowing for variability of reporting of physical features by different observers, and of minimising the number of 'spurious' groups. Evaluation using a test data set of known...

2012
Changha Yu Youngpo Lee Seokho Yoon

In this paper, we propose an enhanced code acquisition scheme for optical code division multiple access (CDMA) systems. By using multiple thresholds, the proposed scheme provides a shorter mean acquisition time (MAT) than that of the conventional multiple-shift (MS) scheme. The simulation results demonstrate that the MAT of the proposed scheme is shorter than that of the conventional MS scheme ...

2018
Wei Liu Hong-Bo Shi Zhe Zhang Sang-Bing Tsai Yuming Zhai Quan Chen Jiangtao Wang

After the Chinese reform and opening up, the construction of economic zones, such as Special Economic Zones, Hi-tech Zones and Bonded Zones, has played an irreplaceable role in China's economic development. Currently, against the background of Chinese economic transition, research on development evaluation of economic zones has become popular and necessary. Similar research usually focuses on o...

2013
Colin W. McInnes Thomas J. Goetz

Synovial osteochondromatosis of the distal radioulnar joint is a rare entity with only 14 cases reported in the literature. Malignant transformation of synovial osteochondromatosis is the most worrisome complication of the disease. It has been described in joints such as the hip and knee but never for the distal radioulnar joint. We report a case of synovial osteochondromatosis of the distal ra...

2017
C. Cybulski W. Kluźniak T. Huzarski D. Wokołorczyk A. Kashyap A. Jakubowska M. Szwiec T. Byrski T. Dębniak B. Górski V. Sopik M. R. Akbari P. Sun J. Gronwald S. A. Narod J. Lubiński D. Dymerska G. Kurzawski K. Tutlewska M. Kuswik H. Rudnicka R. J. Scott R. Billings A. Pławski J. Lubinski T. Gromowski K. Kąklewski W. Marciniak K. Durda M. Lener G. Sukiennicki K. Kaczmarek K. Jaworska-Bieniek K. Paszkowska-Szczur P. Waloszczyk K. Hemminki A. Försti O. Oszurek K. Gugała M. Stawicka Z. Morawiec T. Mierzwa M. Falco H. Janiszewska E. Kilar E. Marczyk B. Kozak-Klonowska M. Siołek D. Surdyka R. Wiśniowski M. Posmyk P. Domagała P. Sun S. A. Narod E. N. Imyanitov M. Muszyńska W. Marciniak K. Prajzendanc N. Peruga A. Morawski M. R. Lener R. J. Scott W. Kluźniak J. Gronwald P. Baszuk C. Cybulski A. Wiechowska-Kozłowska T. Huzarski J. Kładny S. Pietrzak A. Soluch A. Jakubowska J. Lubiński A. Plawski U. R. Rashid H. Naeemi N. Muhammad A. Loya M. A. Yusuf A. Savanevich O. Aszurek A. Mathe M. Wong-Brown W. Locke C. Stirzaker S. G. Braye J. F. Forbes S. Clark K. Avery-Kiejda J. Tomiczek-Szwiec J. Jakubowicz R. Sibilski M. Siołek D. Surdyka R. Wiśniowski R. Posmyk P. Domagała T. Huzarski C. Cybulski J. Lubiński

2014
Abdolrahman Rostamian Hamed Mazoochy Shafieh Movassaghi Seyed Mohammad Javad Mortazavi Elham Sadeghzadeh Fatemeh Shahbazi Hossein Ghanaati

Coexisting ankylosing spondylitis and hereditary multiple exostoses have rarely been reported (three patients) previously. A 27-year-old man with hereditary multiple exostoses is presented as a fourth report. At the age of 15 years, the patient had multiple exostoses around the knee, ankle and shoulder joints. He was diagnosed with ankylosing spondylitis 3 years ago. The patient's sister and hi...

Journal: :Journal of rehabilitation medicine 2017
Jorik Nonnekes Bas van Lith Bart P van de Warrenburg Vivian Weerdesteyn Alexander C H Geurts

INTRODUCTION Balance impairments are common in patients with hereditary spastic paraplegia and are among the most debilitating symptoms, as they frequently result in falls and fall-related injuries. Several features of hereditary spastic paraplegia contribute to balance impairments and multiple treatment options exist. However, an overview of these underlying mechanisms and their treatment is c...

Journal: :Best practice & research. Clinical rheumatology 2003
Merrill D Benson

Hereditary amyloidosis is, in general, a systemic condition related to multiple organ system involvement by beta-structured protein deposits. As such, it often mimics the more common forms of systemic amyloidosis: immunoglobulin light chain (AL, primary) and reactive (AA, secondary). The challenge diagnostically is to recognize hereditary amyloidosis as a distinct entity and then to determine t...

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