Intake, digestibility, ruminal parameters, and microbial protein synthesis in crossbred steers fed diets based on Brachiaria grass silage and sorghum silage Consumo, digestibilidad... oleh F.H.M. Chizzotti, O.G. Pereira, S.C. Valadares Filho, M.L. Chizzotti, M.I. Leão, D.H. Pereira, L.O. Tedeschi

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Beef cattle performance on signal grass pastures deferred and fertilized with nitrogen oleh P.L. Amorim, D.M. Fonseca, M.E.R. Santos, R.M. Pimentel, J.P.P. Rodrigues, F.H.M. Chizzotti, C.G. Vitor

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Development of a web-based register for the Dutch national study on biologicals in juvenile idiopathic arthritis: <url>http://www.abc-register.nl</url> oleh Prince FHM, Ferket IS, Kamphuis SSM, Armbrust W, Ten Cate R, Hoppenreijs EPAH, Koopman-Keemink Y, van Rossum MAJ, van Santen-Hoeufft M, Twilt M, van Suijlekom-Smit LWA

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When and how to stop etanercept after successful treatment of patients with juvenile idiopathic arthritis oleh Prince FHM, Twilt M, Simon SCM, van Rossum MAJ, Armbrust W, Hoppenreijs EPAH, Kamphuis SSM, van Santen-Hoeufft M, Koopman-Keemink Y, Wulffraat N, ten Cate R, van Suijlekom-Smit LWA

Dataset of the phospholipidome and transcriptome of Campylobacter jejuni under different growth conditions oleh Xuefeng Cao, Jos F.H.M. Brouwers, Linda van Dijk, Chris H.A. van de Lest, Craig T. Parker, Steven Huynh, Jos P.H. van Putten, David J. Kelly, Marc M.S.M. Wösten

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Aspects Towards the Anastomotic Healing in Crohn’s Disease: Clinical Approach and Current Gaps in Research oleh F.H.M. Chaim, L.M.V. Negreiros, K.M. Steigleder, N.S.N. Siqueira, L.M. Genaro, P.S.P. Oliveira, C.A.R. Martinez, M.L.S. Ayrizono, J.J. Fagundes, R.F. Leal

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Etanercept in juvenile idiopathic arthritis: Who will benefit? oleh van den Berg JM, Swart JF, Dolman KM, Gorter SL, Koopman-Keemink Y, Twilt M, Hoppenreijs EPAH, ten Cate R, Armbrust W, Prince FHM, Otten MH, Wulffraat NM, van Rossum MAJ, van Suijlekom-Smit LWA

Deploying Digital Health Technologies for Remote Physical Activity Monitoring of Rural Populations With Chronic Neurologic Disease oleh Kimberly J. Waddell, PhD, MSCI, Mitesh S. Patel, MD, MBA, Jayne R. Wilkinson, MD, MSCE, Robert E. Burke, MD, MS, FHM, Dawn M. Bravata, MD, Sreelatha Koganti, BS, Stephanie Wood, BS, James F. Morley, MD, PhD

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Best Definitions of Multimorbidity to Identify Patients With High Health Care Resource Utilization oleh Carole E. Aubert, MD, Jeffrey L. Schnipper, MD, MPH, Marie Roumet, PhD, Pedro Marques-Vidal, MD, PhD, Jérôme Stirnemann, MD, PhD, Andrew D. Auerbach, MD, MPH, Eyal Zimlichman, MD, MSc, Sunil Kripalani, MD, MSc, Eduard E. Vasilevskis, MD, MPH, FHM, Edmondo Robinson, MD, MBA, MSHP, Grant S. Fletcher, MD, MPH, Drahomir Aujesky, MD, MSc, Andreas Limacher, PhD, Jacques Donzé, MD, MSc

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Design and Integration of a Texting Tool to Keep Patients’ Family Members Updated During Hospitalization: Clinicians’ Perspectives oleh Courtenay R Bruce JD, MA, Ashleigh Kamencik-Wright MBA, Natalie Zuniga-Georgy MS, Thomas M Vinh RN, BSN, Hema Shah MSN, BSN, RN, BS, Jamie Shallcross BS, Charlie Giammattei BS, Colleen O’Rourke BS, Mariana Smith MHA, Lindsey Bruchhaus MSN, RN, Yashica Bowens BSN, MBA, MHCM, Kimberley Goode MHA, Lee Ann Arabie BS, Katherine Sauceda BA, Majeedah Pacha MPH, Sandra Martinez MBA, James Chisum MBA, R Benjamin Saldaña DO, FACEP, S Nicholas Desai MD, Melina Awar MD, FACP, FHM, Thomas R Vernon RN, BSN, EdM

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Design and Integration of a Texting Tool to Keep Patients’ Family Members Updated During Hospitalization: Family Members’ Perspectives oleh Courtenay R. Bruce JD, MA, Ashleigh Kamencik-Wright MBA, Natalie Zuniga-Georgy MS, Thomas M. Vinh RN, BSN, Hema Shah MSN, BSN, RN, BS, Jamie Shallcross BS, Charlie Giammattei BS, Colleen O’Rourke BS, Mariana Smith MHA, Lindsey Bruchhaus MSN, RN, Yashica Bowens BSN, MBA, MHCM, Kimberly Goode MA, Lee Ann Arabie BS, Katherine Sauceda BA, Majeedah Pacha MPH, Sandra Martinez MBA, James Chisum BA, R. Benjamin Saldaña DO FACEP, S. Nicholas Desai MD, Melina Awar MD, FACP, FHM, Thomas R. Vernon BSN, EdM

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Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms oleh Yingji Li, Wenjing Tang, Li Kang, Shanshan Kong, Zhao Dong, Dengfa Zhao, Ruozhuo Liu, Shengyuan Yu

"…Abstract Background Mutations in ATP1A2, the gene encoding the α2 subunit of Na+/K+-ATPase, are the main cause of familial hemiplegic migraine type 2 (FHM2). The clinical presentation of FHM2 with mutations in the same gene varies from pure FHM to severe forms with epilepsy and intellectual disability, but the correlation of these symptoms with different ATP1A2 mutations is still unclear. …"
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Familial Hemiplegic Migraine Type 1 Associated with Parkinsonism: A Case Report oleh Marie Bruun, Lena Elisabeth Hjermind, Carsten Thomsen, Else Danielsen, Lise Lykke Thomsen, Lars Hageman Pinborg, Nastaran Khabbazbavani, Joergen Erik Nielsen

"…It is well described that FHM1 can present with cerebellar signs, but parkinsonism has not previously been reported in FHM1 or EA2 even though parkinsonism has been described in SCA6. …"
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Is Neuronal Fatigue the Cause of Migraine? oleh Michael Pusch, Paola Gavazzo

"…Familial hemiplegic migraines (FHM) are monogenic forms of severe migraine, caused by mutations in genes encoding various neuronal and/or astrocytic ion transporting proteins. …"
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Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2. oleh Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari

"…We generated the first FHM2 knock-in mouse model carrying the human W887R mutation in the Atp1a2 orthologous gene. …"
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Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2 oleh Clizia Capuani, Marcello Melone, Angelita Tottene, Luca Bragina, Giovanna Crivellaro, Mirko Santello, Giorgio Casari, Fiorenzo Conti, Daniela Pietrobon

"…A subtype of migraine with aura (familial hemiplegic migraine type 2: FHM2) is caused by loss‐of‐function mutations in α2 Na+,K+ ATPase (α2 NKA), an isoform almost exclusively expressed in astrocytes in adult brain. …"
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5.2 AN ASSOCIATED WITH FAMILIAL HEMIPLEGIC MIGRAINE TYPE 2 MUTATION IN THE ALPHA-2 ISOFORM NA,K-ATPASE DISTURBS VASCULAR RESPONSES IN MOUSE BRAIN oleh Christian Staehr, Lise Hangaard, Karin Lykke-Hartmann, Elena Bouzinova, Christian Aalkjaer, Vladimir Matchkov

"…Heterozygote mice bearing G301R mutation (FHM2) were recently characterized for several behavioral and neuronal abnormalities. …"
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The efficacy of fortified human milk compared to human milk alone for the growth of low birth weight infants oleh Dewi Kumara Wati Ketut, Soetjiningsih Soetjiningsih, Suandi IKG, Hamid H A

"…Objective To evaluate the growth of low birth weight infants fed by fortified human milk (FHM) compared to human milk (HM) alone. Methods Sixty premature infants enrolled in this study and ran- domly assigned to have FHM and HM delivered by infusofeedpump, in parallel, non-blinded controlled trial. …"
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Current status and influential factors for family health management during quarantine: A latent category analysis oleh Guangming Li, Mengying Li, Shuzhen Peng, Ying Wang, Li Ran, Xuyu Chen, Ling Zhang, Sirong Zhu, Qi Chen, Wenjing Wang, Yang Xu, Yubin Zhang, Xiaodong Tan

"…<h4>Conclusions</h4> We found that multiple factors, including gender, household income, and body mass index, were correlated with latent FHM during home quarantine. We conclude that FHM can meaningfully improve individuals’ health. …"
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Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2.1 knockin migraine mice oleh Dania Vecchia, Angelita Tottene, Arn M.J.M. van den Maagdenberg, Daniela Pietrobon

"…Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is caused by gain-of-function mutations in CaV2.1 (P/Q-type) calcium channels. …"
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