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Unleashing the mysterious link between COVID-19 and a famous childhood vasculitis: Kawasaki disease
Unleashing the mysterious link between COVID-19 and a famous childhood vasculitis: Kawasaki disease
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Unleashing the mysterious link between COVID-19 and a famous childhood vasculitis: Kawasaki disease

AbdelMassih, Antoine Fakhry ; AbdelAzeam, Aisha Said ; Ayad, Aya ; Kamel, Aya Yasser ; Khalil, Ayah ; Kotb, Basma ; Waheed, Dina ; Menshawey, Esraa ; Sefein, Fady ; Taha, Farah ; Ismail, Habiba-Allah ; Osman, Ibrahim ; Iskander, John ; El Wakil, Lama ; Rashad, Lara ; Arsanyous, Mariem Badr ; El Shershaby, Meryam ; Mansour, Mina ; Ashraf, Mirette ; Hafez, Nada ; Abuzeid, Nadeen Mohamed ; AbdElSalam, Noheir Mahmoud-Nashaat ; Hafez, Nouran Gamal ; Youssef, Nourhan ; Hozaien, Rafeef ; Saeed, Rana ; Kamel, Dina ; AbdelHameed, Manal Ahmed ; Ali, Salma

The Gazette of the Egyptian Paediatric Association, 2020-07, Vol.68 (1), p.21-7, Article 21 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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2
Scanning electron microscopy for identification of local strain of Aspergillus Parasiticus and its larvicidal efficacy against Aedes Aegypti and non‐target toxicity testing on fingerlings of Hypophthalmichthys Molitrix
Scanning electron microscopy for identification of local strain of Aspergillus Parasiticus and its larvicidal efficacy against Aedes Aegypti and non‐target toxicity testing on fingerlings of Hypophthalmichthys Molitrix
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Scanning electron microscopy for identification of local strain of Aspergillus Parasiticus and its larvicidal efficacy against Aedes Aegypti and non‐target toxicity testing on fingerlings of Hypophthalmichthys Molitrix

Abrar, Amina ; Abbas, Moneeza ; Mehmood, Salma ; Ghani, Nadia ; Fatima, Ammara ; Shahzadi, Rabia

Microscopy research and technique, 2022-09, Vol.85 (9), p.3187-3192 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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3
Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping
Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping
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Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping

Abu Safieh, L ; Aldahmesh, M A ; Shamseldin, H ; Hashem, M ; Shaheen, R ; Alkuraya, H ; Al Hazzaa, S A F ; Al-Rajhi, A ; Alkuraya, F S

Journal of medical genetics, 2010-04, Vol.47 (4), p.236-241 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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4
A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
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A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients

Afzal, Sibtain ; Ramzan, Khushnooda ; Ullah, Sajjad ; Wakil, Salma M ; Jamal, Arshad ; Basit, Sulman ; Waqar, Ahmed Bilal

BMC medical genetics, 2020-01, Vol.21 (1), p.20-20, Article 20 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Novel homozygous sequence variants in the CDH3 gene encoding P-cadherin underlying hypotrichosis with juvenile macular dystrophy in consanguineous families
Novel homozygous sequence variants in the CDH3 gene encoding P-cadherin underlying hypotrichosis with juvenile macular dystrophy in consanguineous families
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Novel homozygous sequence variants in the CDH3 gene encoding P-cadherin underlying hypotrichosis with juvenile macular dystrophy in consanguineous families

Ahmad, Farooq ; Ali, Raja Hussain ; Muhammad, Dost ; Nasir, Abdul ; Umair, Muhammad ; Wakil, Salma M. ; Ramzan, Khushnooda ; Basit, Sulman ; Ahmad, Wasim

EJD. European journal of dermatology, 2016-11, Vol.26 (6), p.610-612 [Periódico revisado por pares]

Paris: John Libbey Eurotext

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6
Enhanced starch hydrolysis by α-amylase using copper oxide nanowires
Enhanced starch hydrolysis by α-amylase using copper oxide nanowires
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Enhanced starch hydrolysis by α-amylase using copper oxide nanowires

Ahmad, Khurshid ; Khan, Suleman ; Yasin, Muhammad Talha ; Hussain, Saddam ; Ahmad, Rasheed ; Ahmad, Naeem ; Ahmed, Muzzamil ; Ghani, Abdul ; Faheem, Muhammad ; Ullah, Hanif ; Hussain, Adil ; Bokhari, Syed Ali Imran

Applied nanoscience, 2021-07, Vol.11 (7), p.2059-2071 [Periódico revisado por pares]

Cham: Springer International Publishing

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7
6th Vacuum and Surface Sciences Conference of Asia and Australia (VASSCAA-6)
6th Vacuum and Surface Sciences Conference of Asia and Australia (VASSCAA-6)
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6th Vacuum and Surface Sciences Conference of Asia and Australia (VASSCAA-6)

Ahsan Bhatti, Javaid ; Hussain, Talib ; Khan, Wakil

Journal of physics. Conference series, 2013-06, Vol.439 (1), p.11001 [Periódico revisado por pares]

Bristol: IOP Publishing

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8
Antioxidant Activity, Acetylcholinesterase, and Carbonic Anhydrase Inhibitory Properties of Novel Ureas Derived from Phenethylamines
Antioxidant Activity, Acetylcholinesterase, and Carbonic Anhydrase Inhibitory Properties of Novel Ureas Derived from Phenethylamines
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Antioxidant Activity, Acetylcholinesterase, and Carbonic Anhydrase Inhibitory Properties of Novel Ureas Derived from Phenethylamines

Aksu, Kadir ; Özgeriş, Bünyamin ; Taslimi, Parham ; Naderi, Ali ; Gülçin, İlhami ; Göksu, Süleyman

Archiv der Pharmazie (Weinheim), 2016-12, Vol.349 (12), p.944-954 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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9
Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism
Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism
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Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism

Alazami, Anas M. ; Al-Owain, Mohammad ; Alzahrani, Fatema ; Shuaib, Taghreed ; Al-Shamrani, Hussain ; Al-Falki, Yahya H. ; Al-Qahtani, Saleh M. ; Alsheddi, Tarfa ; Colak, Dilek ; Alkuraya, Fowzan S.

Human mutation, 2012-10, Vol.33 (10), p.1429-1434 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
TLE6 mutation causes the earliest known human embryonic lethality
TLE6 mutation causes the earliest known human embryonic lethality
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TLE6 mutation causes the earliest known human embryonic lethality

Alazami, Anas M ; Awad, Salma M ; Coskun, Serdar ; Al-Hassan, Saad ; Hijazi, Hadia ; Abdulwahab, Firdous M ; Poizat, Coralie ; Alkuraya, Fowzan S

Genome Biology, 2015-11, Vol.16 (1), p.240-240, Article 240 [Periódico revisado por pares]

England: BioMed Central

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