4,082 results match your criteria: "Vitamin E Deficiency"
Clin Genet
December 2024
Fetal Health Research Center, Hope Generation Foundation, Tehran, Iran.
Ataxia with Vitamin E Deficiency (AVED) is a rare autosomal recessive genetic disorder, that caused by pathogenic variants in the TTPA gene, which encodes the alpha-tocopherol transfer protein. This study investigates eight patients from three consanguineous Iranian families, using exome sequencing (ES) and Sanger sequencing to identify novel pathogenic variants in the TTPA gene. Two variants were identified: c.
View Article and Find Full Text PDFCureus
November 2024
Department of Public Health, The Ministry of Health, Manama, BHR.
Introduction Children with cystic fibrosis (CF) have lipid maldigestion due to pancreatic insufficiency, which causes malabsorption of fat-soluble vitamins. The primary objective of this study was to assess the prevalence of vitamin E deficiency among children with CF. The secondary objective was to examine the correlation between vitamin E levels with demographic data, laboratory findings, and the number of pulmonary exacerbations.
View Article and Find Full Text PDFMol Nutr Food Res
December 2024
Aix-Marseille Université, INRAE, INSERM, C2VN, Marseille, France.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
November 2024
Reproductive Medicine Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China.
Mymensingh Med J
October 2024
Dr Sukumar Mondithoka, Assistant Professor, Department of Medicine, AIIMS Bhopal, India; E-mail:
Zhonghua Wei Chang Wai Ke Za Zhi
September 2024
Department of Bariatric and Metabolic Surgery, China-Japan Union Hospital, Jilin University, Changchun 130033, China.
Ann Med
December 2024
Department of Tuberculosis Control and Prevention, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, China.
Cureus
June 2024
Department of Neurology, Mohammed Vl University Hospital, Faculty of Medicine and Pharmacy, Mohammed First University, Oujda, MAR.
Eur J Gastroenterol Hepatol
October 2024
Department of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, University of Florida, Gainesville.
J Clin Med
June 2024
Servicio de Medicina Interna, Facultad de Medicina, Instituto de Investigación Sanitaria del Hospital San Carlos, Hospital Clínico San Carlos, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Clin Nutr ESPEN
October 2024
Department of Pediatrics, College of Medicine, University of Cincinnati, USA; Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, USA.
Cureus
May 2024
Oral Medicine and Radiology, Sharad Pawar Dental College and Hospital, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Zhonghua Er Ke Za Zhi
June 2024
Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai 201102, China.
To summarize the genotype and clinical characteristics of chylomicron retention disease (CMRD) caused by secretion associated Ras related GTPase 1B (SAR1B) gene variations. Clinical data and genetic testing results of 2 children with CMRD treated at Children's Hospital of Fudan University and Jiangxi Provincial Children's Hospital from May 2022 to July 2023 were summarized. To provide an overview of the clinical and genetic characteristics of CMRD caused by SAR1B gene variations, all of the literature was searched and reviewed from China National Knowledge Infrastructure, Wanfang Data Knowledge Service Platform, China VIP database, China Biology Medicine disc and PubMed database (up to January 2024) with "chylomicron retention disease" "Anderson disease" or "Anderson syndrome" as the search terms.
View Article and Find Full Text PDFFree Radic Biol Med
August 2024
Research Center for Advanced Science and Technology, The University of Tokyo, Komaba, Tokyo, Japan. Electronic address:
Vet J
June 2024
Center for Equine Health, School of Veterinary Medicine, University of California, Davis, CA, USA; Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA, USA. Electronic address:
Protein Cell
November 2024
Institute for Immunology and School of Basic Medicine, Tsinghua University, Beijing 100084, China.
J Vet Intern Med
May 2024
Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, California 95616, USA.
Foods
March 2024
Hunan Key Laboratory of Grain-Oil Deep Process and Quality Control, Hunan Key Laboratory of Forestry Edible Resources Safety and Processing, Central South University of Forestry and Technology, Changsha 410004, China.
Free Radic Biol Med
March 2024
BASF SE, Nutrition & Health Division, Ludwigshafen am Rhein, Germany.
Free Radic Biol Med
March 2024
Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331, USA.
Ann Indian Acad Neurol
September 2023
Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Vet Radiol Ultrasound
March 2024
Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
J Neurogenet
March 2024
Molecular Neurobiology and Neuropathology Department, National Institute Mongi Ben Hamida of Neurology, Tunisia.
J Mov Disord
April 2024
Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Neurogenetics
January 2024
Department of Ophthalmology, IHU FOReSIGHT, Hôpital Universitaire Pitié-Salpêtrière, Sorbonne Université, 47-83 Boulevard de l'Hôpital, 75013, Paris, France.