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Refinado por: assunto: eng remover Base de dados/Biblioteca: ScienceDirect (Online service) remover
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1
Tuneable double negative (DNG) Tri-Hexagonal split ring resonator metamaterial for 5G application
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Artigo
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Tuneable double negative (DNG) Tri-Hexagonal split ring resonator metamaterial for 5G application

Arbaatun Adawiah, Nurul ; Salem Al-Bawri, Samir ; Mohd Sahar, Norsuzlin ; Tariqul Islam, Mohammad ; Singh, Mandeep S.J.

Journal of magnetism and magnetic materials, 2024-05, Vol.598, p.172057, Article 172057 [Periódico revisado por pares]

Elsevier B.V

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2
Recording and manipulation of vagus nerve electrical activity in chronically instrumented unanesthetized near term fetal sheep
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Artigo
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Recording and manipulation of vagus nerve electrical activity in chronically instrumented unanesthetized near term fetal sheep

Castel, Aude ; Burns, Patrick M. ; Benito, Javier ; Liu, Hai L. ; Kuthiala, Shikha ; Durosier, Lucien D. ; Frank, Yael ; Cao, Mingju ; Paquet, Marilène ; Fecteau, Gilles ; Desrochers, André ; Frasch, Martin G.

Journal of neuroscience methods, 2021-08, Vol.360, p.109257-109257, Article 109257 [Periódico revisado por pares]

Elsevier B.V

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3
Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2)
Material Type:
Artigo
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Curaçao diagnostic criteria for hereditary hemorrhagic telangiectasia is highly predictive of a pathogenic variant in ENG or ACVRL1 (HHT1 and HHT2)

McDonald, Jamie ; Bayrak-Toydemir, Pinar ; DeMille, Desiree ; Wooderchak-Donahue, Whitney ; Whitehead, Kevin

Genetics in medicine, 2020-07, Vol.22 (7), p.1201-1205 [Periódico revisado por pares]

United States: Elsevier Limited

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4
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1
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Artigo
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Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1

Snellings, Daniel A. ; Gallione, Carol J. ; Clark, Dewi S. ; Vozoris, Nicholas T. ; Faughnan, Marie E. ; Marchuk, Douglas A.

American journal of human genetics, 2019-11, Vol.105 (5), p.894-906 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers
Material Type:
Artigo
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Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers

SABBÀ, C. ; PASCULLI, G. ; LENATO, G. M. ; SUPPRESSA, P. ; LASTELLA, P. ; MEMEO, M. ; DICUONZO, F. ; GUANTI, G.

Journal of thrombosis and haemostasis, 2007-06, Vol.5 (6), p.1149-1157 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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