Results 101 to 110 of about 31,177 (302)

Assessment of Genetic Correlations Between Tobacco or Alcohol Use and Neurodegenerative Diseases Using East Asian Genetic Ancestry Genome‐Wide Association Study Results

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Alzheimer's disease (AD) and Parkinson's disease (PD) are the most prevalent late‐onset neurodegenerative diseases worldwide. Both are influenced in part by genetic factors and are currently incurable. Tobacco and alcohol, the two most common substances used among the general adult population, are potential AD/PD risk factors and are also ...
Linda Wang, Wiame Belbellaj, Frida Lona‐Durazo, Sarah A. Gagliano Taliun   +3 more
wiley   +1 more source

أثر الأنظمة القضائية الجديدة في الشروط الإجرائية والموضوعية للمدعي والمدعى عليه في نظام المعاملات المدنية السعودي الصادر بالمرسوم الملكي رقم [م/191] وتاريخ 29/11/1444هـ، ونظام الأحوال الشخصية الصادر بالمرسوم الملكي رقم [م/73] وتاريخ 6/8/1443هـ والقرارات ذات العلاقة مقارناً بالفقه [PDF]

مجلة البحوث الفقهیة والقانونیة
تناول هذا البحث تعريف المدعي والمدعى عليه في النظام السعودي، والفقه الإسلامي، وأجرى المقارنة بينهما، كما تطرق في المطلب الأول إلى شروط المدعي في النظام السعودي والفقه الإسلامي والمقارنة بينهما وأثر الأنظمة القضائية الجديدة فيها وحيث توصلت الدراسة إلى أن ...
عبدالله بن علي العَمْري
doaj   +1 more source

Practice and Procedures - costs - offer to settle by plaintiff under UCPR r360 for amount of claim plus costs

, 2002
In JLG Industries Inc v Teetree Pty Ltd [2002] QDC 031 the court considered the implications in terms of costs of an offer to settle by the plaintiff under the UCPR where the element of compromise involved only acceptance of the amount of claim without ...
Jackson, Sheryl
core  

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Introducing a Presumption Rule to Reduce the Burden of Proof in Trade Secret Infringement Legislation: Legislation Examples from China and Japan

Journal of Intellectual Property
In civil litigation, the plaintiff bears the burden of proof of holding the defendant liable for damages. However, in modern cases such as medical malpractice, pollution, and product liability, it is difficult for the plaintiff to bear the burden of ...
Dae Soon Jung
doaj   +1 more source

In Supreme Court, August term, 1923, no. 69, Jewett & Sherman Company, a corporation, plaintiff and respondent vs. Rosenberg Brothers & Company, a corporation, defendant and appellant brief of plaintiff and respondant /

, 1923
Action by the plaintiff to recover from the defendant certain amounts paid for honey, from Arizona, alleged to have been of inferior quality and grade.
Charles C. Miller Memorial Apicultural Library. WU, Wisconsin. Supreme Court., Jewett and Sherman Company (Milwaukee, Wis.), plaintiff., Rosenberg Bros. and Company (San Francisco, Calif.), defendant.   +3 more
core  

Posthumously Diagnosed Myhre Syndrome Presenting With Pleural Remodeling and Endometrial Cancer

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (OMIM 139210) is a genetic condition defined by neurodevelopmental disability, characteristic facial features, and multisystem proliferative fibrosis. While various types of lung disease have been reported, pleural remodeling leading to restrictive lung disease has not yet been described.
Jeanette Saffir, Karee Morgan, Karigynn Chaimson, Blake E. Funke, Kim L. Sandler, Melissa Hogan, Thomas Cassini   +6 more
wiley   +1 more source

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen, Kristin Ørstavik, Unni Steen, Mathias Toft, Cathrine Brunborg, Lena Lande Wekre   +5 more
wiley   +1 more source

Reply Brief for Plaintiff-Appellant Guy Zappulla

, 2015
Betsy Ginsberg filed a Reply Brief for Plaintiff-Appellant Guy ...
Ginsberg, Betsy
core   +3 more sources

The Legislation for Providing Animal Access in Australian Residential Aged Care: It's Not a Zoo

Australian Journal of Social Issues, EarlyView.
ABSTRACT Providing meaningful animal contact to residential aged care facility (RACF) residents is problematic due to a lack of animal policies and National Guidelines. This paper examines how Australian Legislation could influence access to animal contact in RACFs and aims to answer the question, ‘Could current Legislation facilitate the development ...
Wendy Newton, Tania Signal, Jenni A. Judd   +2 more
wiley   +1 more source