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Search Results - AlBatti, Turki H.
Search Results - AlBatti, Turki H.
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Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative
by
Bashiri, Fahad A
,
Albatti, Turki H
,
Hamad, Muddathir H
,
Al-Joudi, Haya F
,
Daghash, Hadeel F
,
Al-Salehi, Saleh M
,
Varnham, Jeremy L
,
Alhaidar, Fatimah
,
Almodayfer, Omar
,
Alhossein, Abdulkarim
,
Aldhalaan, Hesham
,
Ad-Dab'bagh, Yasser A
,
Al Backer, Nouf
,
Altwaijri, Waleed
,
Alburikan, Khalid
,
Buraik, Maysaa W
,
Ghaziuddin, Mohammad
,
Nester, Michael J
,
Wahabi, Hayfaa A
,
Alhabib, Samia
,
Jamal, Amr A
,
Amer, Yasser S
Published in
Child and adolescent psychiatry and mental health
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A de novo ATXN2L variant in a child with developmental delay and macrocephaly
by
Alzahrani, Fatema
,
Albatti, Turki H.
,
Alkuraya, Fowzan S.
Published in
American journal of medical genetics. Part A
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PLXNA2 as a candidate gene in patients with intellectual disability
by
Altuame, Fadie D.
,
Shamseldin, Hanan E.
,
Albatti, Turki H.
,
Hashem, Mais
,
Ewida, Nour
,
Abdulwahab, Firdous
,
Alkuraya, Fowzan S.
Published in
American journal of medical genetics. Part A
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Prevalence of autism spectrum disorder among Saudi children between 2 and 4 years old in Riyadh
by
AlBatti, Turki H.
,
Alsaghan, Lamya B.
,
Alsharif, Malak F.
,
Alharbi, Jwaher S.
,
BinOmair, Alanoud I.
,
Alghurair, Hadeel A.
,
Aleissa, Ghadah A.
,
Bashiri, Fahad A.
Published in
Asian journal of psychiatry
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Prevalence of attention deficit hyperactivity disorder among primary school-children in Riyadh, Saudi Arabia; 2015–2016
by
Albatti, Turki H.
,
Alhedyan, Zhour
,
Alnaeim, Norah
,
Almuhareb, Anjod
,
Alabdulkarim, Jawaher
,
Albadia, Rawan
,
Alshahrani, Khawla
Published in
International journal of pediatrics & adolescent medicine
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PLXNA2 as a candidate gene in patients with intellectual disability
by
Altuame, Fadie D
,
Shamseldin, Hanan E
,
Albatti, Turki H
,
Hashem, Mais
,
Ewida, Nour
,
Abdulwahab, Firdous
,
Alkuraya, Fowzan S
Published in
American journal of medical genetics. Part A
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