scholarly journals Subretinal Gene Therapy of Mice With Bardet-Biedl Syndrome Type 1

2013 ◽  
Vol 54 (9) ◽  
pp. 6118 ◽  
Author(s):  
Seongjin Seo ◽  
Robert F. Mullins ◽  
Alina V. Dumitrescu ◽  
Sajag Bhattarai ◽  
Daniel Gratie ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Syndrome Type ◽  
Bardet Biedl Syndrome

scholarly journals Clinical characteristics and ultra-widefield fundus image analysis of two siblings with Bardet-Biedl syndrome type 1 p.Met390Arg variant

2020 ◽  
Vol 20 ◽  
pp. 100914
Author(s):  
Sofia M. Muns ◽  
Lorena A. Montalvo ◽  
Jose G. Vargas Del Valle ◽  
Meliza Martinez ◽  
Armando L. Oliver ◽  
...  
Keyword(s):  
Image Analysis ◽  
Clinical Characteristics ◽  
Syndrome Type ◽  
Fundus Image ◽  
Bardet Biedl Syndrome

W1862 Proteoliposomes Containing Sendai Virus F-Glycoprotein for Hepatocyte-Targeted Gene Therapy of the Gunn Rat Model of Crigler-Najjar Syndrome Type 1

2008 ◽  
Vol 134 (4) ◽  
pp. A-840 ◽  
Author(s):  
Xia Wang ◽  
Debi P. Sarkar ◽  
Prashant Mani ◽  
Clifford J. Steer ◽  
Betsy T. Kren ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Rat Model ◽  
Sendai Virus ◽  
Syndrome Type ◽  
Gunn Rat ◽  
Targeted Gene Therapy

scholarly journals TUDCA Slows Retinal Degeneration in Two Different Mouse Models of Retinitis Pigmentosa and Prevents Obesity in Bardet-Biedl Syndrome Type 1 Mice

2012 ◽  
Vol 53 (1) ◽  
pp. 100 ◽  
Author(s):  
Arlene V. Drack ◽  
Alina V. Dumitrescu ◽  
Sajag Bhattarai ◽  
Daniel Gratie ◽  
Edwin M. Stone ◽  
...  
Keyword(s):  
Retinitis Pigmentosa ◽  
Retinal Degeneration ◽  
Mouse Models ◽  
Syndrome Type ◽  
Bardet Biedl Syndrome

Gene Therapy with Bilirubin-UDP-Glucuronosyltransferase in the Gunn Rat Model of Crigler-Najjar Syndrome Type 1

1998 ◽  
Vol 9 (4) ◽  
pp. 497-505 ◽  
Author(s):  
Qianhong Li ◽  
Sidney S. Murphree ◽  
Sharon S. Willer ◽  
Roberto Bolli ◽  
Brent A. French
Keyword(s):  
Gene Therapy ◽  
Rat Model ◽  
Syndrome Type ◽  
Gunn Rat ◽  
Udp Glucuronosyltransferase

A Step Toward Liver Gene Therapy: Efficient Correction of the Genetic Defect of Hepatocytes Isolated From a Patient With Crigler-Najjar Syndrome Type 1 With Lentiviral Vectors

2009 ◽  
Vol 87 (7) ◽  
pp. 1006-1012 ◽  
Author(s):  
Jacques Birraux ◽  
Olivier Menzel ◽  
Barbara Wildhaber ◽  
Caty Jond ◽  
Tuan Huy Nguyen ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Genetic Defect ◽  
Lentiviral Vectors ◽  
Syndrome Type ◽  
Liver Gene

Challenges in the Diagnostic Conceptualization of CRPS-1 (Formerly Conceptualized as RSD)

2006 ◽  
Vol 11 (2) ◽  
pp. 1-3, 9-12
Author(s):  
Robert J. Barth ◽  
Tom W. Bohr
Keyword(s):  
Clinical Practice ◽  
Complex Regional Pain Syndrome ◽  
Somatoform Disorders ◽  
International Association ◽  
Pain Syndrome ◽  
Somatoform Disorder ◽  
Syndrome Type ◽  
Previous Issue

Abstract From the previous issue, this article continues a discussion of the potentially confusing aspects of the diagnostic formulation for complex regional pain syndrome type 1 (CRPS-1) proposed by the International Association for the Study of Pain (IASP), the relevance of these issues for a proposed future protocol, and recommendations for clinical practice. IASP is working to resolve the contradictions in its approach to CRPS-1 diagnosis, but it continues to include the following criterion: “[c]ontinuing pain, which is disproportionate to any inciting event.” This language only perpetuates existing issues with current definitions, specifically the overlap between the IASP criteria for CRPS-1 and somatoform disorders, overlap with the guidelines for malingering, and self-contradiction with respect to the suggestion of injury-relatedness. The authors propose to overcome the last of these by revising the criterion: “[c]omplaints of pain in the absence of any identifiable injury that could credibly account for the complaints.” Similarly, the overlap with somatoform disorders could be reworded: “The possibility of a somatoform disorder has been thoroughly assessed, with the results of that assessment failing to produce any consistencies with a somatoform scenario.” The overlap with malingering could be addressed in this manner: “The possibility of malingering has been thoroughly assessed, with the results of that assessment failing to produce any consistencies with a malingering scenario.” The article concludes with six recommendations, and a sidebar discusses rating impairment for CRPS-1 (with explicit instructions not to use the pain chapter for this purpose).

Management of Complex Regional Pain Syndrome Type 1 with Barbiturate Coma Therapy -A case report-

2006 ◽  
Vol 19 (2) ◽  
pp. 213
Author(s):  
Tae Kyu Park ◽  
Kyung Ream Han ◽  
Dong Wook Shin ◽  
Young Joo Lee ◽  
Chan Kim
Keyword(s):  
Case Report ◽  
Complex Regional Pain Syndrome ◽  
Pain Syndrome ◽  
Syndrome Type ◽  
Barbiturate Coma

Complex regional pain syndrome type 1 in young adults

2018 ◽  
Vol 60 (3) ◽  
pp. 78
Author(s):  
Yasin Demir ◽  
Ümüt Güzelküçük ◽  
Serdar Kesikburun ◽  
Berke Aras ◽  
Mehmet Ali Taşkaynatan ◽  
...  
Keyword(s):  
Young Adults ◽  
Complex Regional Pain Syndrome ◽  
Pain Syndrome ◽  
Syndrome Type
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