Results 91 to 100 of about 81,923 (299)

EFEKTIFITAS ALOE VERA (ALOE BARBADENSIS MILLEER) DALAM PENANGANAN HAND FOOT SYNDROME PADA PASIEN KANKER PAYUDARA YANG MENDAPAT TERAPI CAPECITABINE PER ORAL [PDF]

, 2018
Latar Belakang: Kemoterapi merupakan salah satu terapi yang sudah banyak dipakai untuk pengobatan kanker yang terbukti meningkatkan survival rate pasien. Namun, kemoterapi dapat memberikan efek samping. Salah satunya ialah Hand foot syndrome.
Hapsari, Paramita Nindya, Prajoko, Yan Wisnu, Budijitno , Selamat   +2 more
core  

Rett Syndrome: Revised diagnostic criteria and nomenclature [PDF]

, 2010
Objective: Rett syndrome (RTT) is a severe neurodevelopmental disease that affects approximately 1 in 10,000 live female births and is often caused by mutations in Methyl-CpG-binding protein 2 (MECP2). Despite distinct clinical features, the accumulation
Leonard, Helen, Zappella, M., Angus J. Clarke, Bailey, Mark E. S., Daniel G. Glaze, Clarke, A.J., Zappella, Michele, Kaufmann, Walter E., Neul, J.L., null Jeffrey L. Neul, John Christodoulou, N. Carolyn Schanen, Christodoulou, John, Percy, Alan K., Leonard, H., Michele Zappella, Walter E. Kaufmann, Mark E. S. Bailey, Neul, Jeffrey L., Kaufmann, W.E., RENIERI, ALESSANDRA, Schanen, N. Carolyn, Glaze, Daniel G., Bailey, M.E., Clarke, Angus John, Helen Leonard, Bailey, M.E.S., Bahi Buisson, N., Christodoulou, J., Peter Huppke, Percy, A.K., Bahi-Buisson, N., null null, RettSearch Consortium, MARI, FRANCESCA, Renieri, A., Alessandra Renieri, Nadia Bahi-Buisson, Bahi-Buisson, Nadia, Alan K. Percy, Huppke, Peter, Clarke, Angus J., Glaze, D.G., Schanen, N.C., Huppke, P.   +44 more
core   +1 more source

A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita—Characterization Using Urine‐Derived Cells

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is defined as the presence of joint contractures affecting at least two body regions at birth. Three different ERGIC1 variants have been reported in individuals with AMC. Here, we report on a 16‐year‐old male with a homozygous ERGIC1 c.250+1G>A variant that was classified as a variant of uncertain ...
Lauren Kerr, Paul McKay, Juliana Marulanda, Zenghui Wu, Reggie Hamdy, Sena Tavukcu, Noémi Dahan‐Oliel, Frank Rauch   +7 more
wiley   +1 more source

Preoperative Imaging of Charcot Neuroarthropathy in Diabetic Patients: Comparison of Ring PET, Hybrid PET, and Magnetic Resonance Imaging [PDF]

, 2004
Introduction: The treatment of Charcot neuroarthropathy in the feet of diabetic patients has undergone fundamental changes in the last few years. Formerly, treatment was almost exclusively limited to nonoperative measures; since the late 1990s, however ...
Tiling, Reinhold, Krolak, Christoph, Dresel, Stefan, Höpfner, Stefan, Kessler, Stefan, Brinkbäumer, Kirsten, Hahn, Klaus   +6 more
core   +1 more source

The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is a group of rare congenital conditions, characterized by multiple joint contractures but may involve any body system including central nervous system. AMC is etiologically heterogeneous, with over 400 genetic and many non‐genetic causes implicated in its prenatal development.
Shahrzad Nematollahi, Noa Bouzaglo, Victoria Castillo Sanchez, Johanna I. P. de‐Vries, Klaus Dieterich, Alicja Fafara, Isabel Filges, Philip Giampietro, Göknur Haliloğlu, Judith Hall, Coleman Hilton, Remco Jansen, Valentina Maestri, Carolina Navalon, Daniel Natera de Benito, Tony Pan, Ani Samargian, Bonita Sawatzky, Harold van Bosse, Paul A. Trainor, Noémi Dahan‐Oliel   +20 more
wiley   +1 more source

Pregabalin for Treatment of Docetaxel-Related Hand-Foot Syndrome

, 2019
Hand-foot syndrome (HFS), also known as palmar-plantar erythrodysesthesia, is a painful, often debilitating condition related to the use of various chemotherapies.
Orare, Kelvin, Karar, Sayed, Nambafu, Jamila, Mwanzi, Sitna   +3 more
core   +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

Anti‐inflammatory and osteogenic effects of transcutaneous electrical nerve stimulation in knee osteoarthritis rats via the regulation of the intestinal microbiota

Animal Models and Experimental Medicine, EarlyView.
Transcutaneous electrical nerve stimulation (TENS) improved knee osteoarthritis (KOA) in rats by regulating interleukin‐1β (IL‐1β), IL‐6, and IL‐8 expressions and the bone morphogenetic protein 2 (BMP‐2)/transforming growth factor β (TGF‐β) signaling pathway.
Yan Sun, Tong Ma, Ran Chen, Lan Shen, Xun Tang, Zhiqiang Shen, Hongbin Zhao   +6 more
wiley   +1 more source

Animal models of idiopathic membranous nephropathy: Recent advances and future perspectives

Animal Models and Experimental Medicine, EarlyView.
This review focuses on the evolution of idiopathic membranous nephropathy (IMN) animal models from traditional approaches (Heymann nephritis, C‐BSA, APA) to antigen‐specific models (PLA2R, THSD7A), critically evaluating their advances and limitations in replicating human IMN pathology.
Qiuying Liu, Huixian Bian, Jianhua Liu, Lina Wu, Zhijie Zhang, Hongli Zhao, Xiaosong Qin   +6 more
wiley   +1 more source

Ehlers-Danlos syndrome with infective endocarditis: A case report with literature review

IDCases, 2019
We report a patient with Ehlers-Danlos syndrome and mitral valve infective endocarditis. The case was complicated due to multiorgan involvement and initially diagnosed as hand-foot-and-mouth disease.
Yang Jiao, Mark S. Rasnake, Michael T. McCormack, J. Francis Turner   +3 more
doaj   +1 more source