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Compact metamaterial-based single/double-negative/near-zero index resonator for 5G sub-6 GHz wireless applications
Compact metamaterial-based single/double-negative/near-zero index resonator for 5G sub-6 GHz wireless applications
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Compact metamaterial-based single/double-negative/near-zero index resonator for 5G sub-6 GHz wireless applications

Ibrahim, Sura Khalil ; Al-Bawri, Samir Salem ; Singh, Mandeep Jit ; Ibrahim, Husam Hamid ; Islam, Mohammad Tariqul ; Islam, Md Shabiul ; Abdulkawi, Wazie M ; Sheta, Abdel-Fattah A

Scientific reports, 2024-06, Vol.14 (1), p.12834-12834, Article 12834 [Periódico revisado por pares]

London: Nature Publishing Group

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Tunable Compact Metamaterial-Based Double-Negative/Near-Zero Index Resonator for 6G Terahertz Wireless Applications
Tunable Compact Metamaterial-Based Double-Negative/Near-Zero Index Resonator for 6G Terahertz Wireless Applications
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Tunable Compact Metamaterial-Based Double-Negative/Near-Zero Index Resonator for 6G Terahertz Wireless Applications

Musaed, Alya Ali ; Al-Bawri, Samir Salem ; Islam, Mohammad Tariqul ; Al-Gburi, Ahmed Jamal Abdullah ; Singh, Mandeep Jit

Materials, 2022-08, Vol.15 (16), p.5608 [Periódico revisado por pares]

Basel: MDPI AG

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3
Double-E-Triple-H-Shaped NRI-Metamaterial for Dual-Band Microwave Sensing Applications
Double-E-Triple-H-Shaped NRI-Metamaterial for Dual-Band Microwave Sensing Applications
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Double-E-Triple-H-Shaped NRI-Metamaterial for Dual-Band Microwave Sensing Applications

Hossain, Shafayat ; Iquebal Hossain Patwary, Md ; Sunbeam Islam, Sikder ; Mahmud, Sultan ; Binti Misran, Norbahiah ; F. Almutairi, Ali ; Tariqul Islam, Mohammad

Computers, materials & continua, 2022, Vol.71 (3), p.5817-5836

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Brain arteriovenous malformation in hereditary hemorrhagic telangiectasia: Recent advances in cellular and molecular mechanisms
Brain arteriovenous malformation in hereditary hemorrhagic telangiectasia: Recent advances in cellular and molecular mechanisms
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Brain arteriovenous malformation in hereditary hemorrhagic telangiectasia: Recent advances in cellular and molecular mechanisms

Drapé, Elise ; Anquetil, Typhaine ; Larrivée, Bruno ; Dubrac, Alexandre

Frontiers in human neuroscience, 2022-11, Vol.16, p.1006115-1006115 [Periódico revisado por pares]

Switzerland: Frontiers Research Foundation

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5
Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions
Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions
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Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions

Snodgrass, Ryan O ; Chico, Timothy J A ; Arthur, Helen M

Genes, 2021-01, Vol.12 (2), p.174 [Periódico revisado por pares]

Switzerland: MDPI AG

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6
Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia
Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia
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Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia

Vorselaars, Veronique M M ; Hosman, Anna E ; Westermann, Cornelis J J ; Snijder, Repke J ; Mager, Johannes J ; Goumans, Marie-Jose ; Post, Marco C

International journal of molecular sciences, 2018-10, Vol.19 (10), p.3203 [Periódico revisado por pares]

Switzerland: MDPI

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7
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG
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Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG

Villa, Davide ; Cinnante, Claudia ; Valcamonica, Gloria ; Manenti, Giulia ; Lanfranconi, Silvia ; Colombi, Annalisa ; Ghione, Isabella ; Saetti, Maria Cristina ; D'Amico, Mario ; Bonato, Sara ; Bresolin, Nereo ; Comi, Giacomo Pietro ; Ronchi, Dario

BMC neurology, 2020-08, Vol.20 (1), p.1-316, Article 316 [Periódico revisado por pares]

London: BioMed Central Ltd

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8
Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia
Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia
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Mutational and clinical spectrum of Japanese patients with hereditary hemorrhagic telangiectasia

Kitayama, Kana ; Ishiguro, Tomoya ; Komiyama, Masaki ; Morisaki, Takayuki ; Morisaki, Hiroko ; Minase, Gaku ; Hamanaka, Kohei ; Miyatake, Satoko ; Matsumoto, Naomichi ; Kato, Masaru ; Takahashi, Toru ; Yorifuji, Tohru

BMC medical genomics, 2021-12, Vol.14 (1), p.288-288, Article 288 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family
Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family
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Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family

Zevallos-Morales, Alejandro ; Murillo, Alexis ; Dueñas-Roque, Milagros M ; Prötzel, Ana ; Venegas-Tresierra, Luis ; Ángeles-Villalba, Verónica ; Guevara-Cruz, Miguel ; Chávez-Gil, Ada ; Fujita, Ricardo ; Guevara-Fujita, Maria L

Genetics and molecular biology, 2020-01, Vol.43 (1), p.e20190126-e20190126 [Periódico revisado por pares]

Brazil: Sociedade Brasileira de Genética

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Ocular lesions in hereditary hemorrhagic telangiectasia: genetics and clinical characteristics
Ocular lesions in hereditary hemorrhagic telangiectasia: genetics and clinical characteristics
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Ocular lesions in hereditary hemorrhagic telangiectasia: genetics and clinical characteristics

Gómez-Acebo, Inés ; Prado, Sara Rodríguez ; De La Mora, Ãngel ; Puente, Roberto Zarrabeitia ; de la Roza Varela, Beatriz ; Dierssen-Sotos, Trinidad ; Llorca, Javier

Orphanet journal of rare diseases, 2020-06, Vol.15 (1), p.1-168, Article 168 [Periódico revisado por pares]

London: BioMed Central Ltd

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