Výsledky vyhledávání - Farooq Naeem

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  1. 1
    Tackling nonadherence in psychiatric disorders: current opinion

    Tackling nonadherence in psychiatric disorders: current opinion Autor Saeed Farooq, Farooq Naeem

    Vydáno 2014
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  2. 2
    An evidence-based framework to culturally adapt cognitive behaviour therapy

    An evidence-based framework to culturally adapt cognitive behaviour therapy Autor Shanaya Rathod, Peter Phiri, Farooq Naeem

    Vydáno 2019
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    Artigo
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  3. 3
    COPING WITH COVID-19: URGENT NEED FOR BUILDING RESILIENCE THROUGH COGNITIVE BEHAVIOUR THERAPY

    COPING WITH COVID-19: URGENT NEED FOR BUILDING RESILIENCE THROUGH COGNITIVE BEHAVIOUR THERAPY Autor Farooq Naeem, Muhammad Irfan, Afzal Javed

    Vydáno 2020
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    Artigo
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  4. 4
    Psychologists experience of cognitive behaviour therapy in a developing country: a qualitative study from Pakistan

    Psychologists experience of cognitive behaviour therapy in a developing country: a qualitative study from Pakistan Autor Farooq Naeem, Mary Gobbi, Muhammad Ayub, David Kingdon

    Vydáno 2010
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    Artigo
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  5. 5
    Preliminary Evaluation of Culturally Sensitive CBT for Depression in Pakistan: Findings from Developing Culturally-Sensitive CBT Project (DCCP)

    Preliminary Evaluation of Culturally Sensitive CBT for Depression in Pakistan: Findings from Developing Culturally-Sensitive CBT Project (DCCP) Autor Farooq Naeem, Waquas Waheed, Mary Gobbi, Muhammad Ayub, David Kingdon

    Vydáno 2010
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  6. 6
    Barriers to using clozapine in treatment-resistant schizophrenia: systematic review

    Barriers to using clozapine in treatment-resistant schizophrenia: systematic review Autor Saeed Farooq, Abid Choudry, Dan Cohen, Farooq Naeem, Muhammad Ayub

    Vydáno 2018
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  7. 7
    Schizophrenia medication adherence in a resource-poor setting: randomised controlled trial of supervised treatment in out-patients for schizophrenia (STOPS)

    Schizophrenia medication adherence in a resource-poor setting: randomised controlled trial of supervised treatment in out-patients for schizophrenia (STOPS) Autor Saeed Farooq, Zahid Nazar, Muhammad Irfan, Javed Akhter, Ejaz Gul, Uma M. Irfan, Farooq Naeem

    Vydáno 2011
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  8. 8
    Mental Health Service Provision in Low- and Middle-Income Countries

    Mental Health Service Provision in Low- and Middle-Income Countries Autor Shanaya Rathod, Narsimha R. Pinninti, Muhammad Irfan, Paul Gorczynski, Pranay Rathod, Lina Gega, Farooq Naeem

    Vydáno 2017
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  9. 9
    The current status of culturally adapted mental health interventions: a practice-focused review of meta-analyses

    The current status of culturally adapted mental health interventions: a practice-focused review of meta-analyses Autor Shanaya Rathod, Lina Gega, Amy Degnan, Jennifer Pikard, Tasneem Khan, Nusrat Husain, Tariq Munshi, Farooq Naeem

    Vydáno 2018
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  10. 10
    mHealth based interventions for the assessment and treatment of psychotic disorders: a systematic review

    mHealth based interventions for the assessment and treatment of psychotic disorders: a systematic review Autor Nadeem Gire, Saeed Farooq, Farooq Naeem, Joy Duxbury, Mick McKeown, P. Kundi, Imran B. Chaudhry, Nusrat Husain

    Vydáno 2017
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  11. 11
    Brief psychological intervention after self-harm: randomised controlled trial from Pakistan

    Brief psychological intervention after self-harm: randomised controlled trial from Pakistan Autor Nusrat Husain, Salahuddin Afsar, Jamal Ara, Hina Fayyaz, Raza-Ur Rahman, Barbara Tomenson, Munir Hamirani, Nasim Chaudhry, Batool Fatima, Meher Husain, Farooq Naeem, Imran B. Chaudhry

    Vydáno 2014
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  12. 12
    CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa

    CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa Autor Abdul Noor, Christian Windpassinger, Megha Patel, Beata Stachowiak, Anna Mikhailov, Matloob Azam, Muhammad Irfan, Zahid Kamal Siddiqui, Farooq Naeem, Andrew D. Paterson, Muhammad Lutfullah, John B. Vincent, Muhammad Ayub

    Vydáno 2008
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  13. 13
    A qualitative study to explore views of patients’, carers’ and mental health professionals’ to inform cultural adaptation of CBT for psychosis (CBTp) in China

    A qualitative study to explore views of patients’, carers’ and mental health professionals’ to inform cultural adaptation of CBT for psychosis (CBTp) in China Autor Weihui Li, Li Zhang, Xuerong Luo, Bangshan Liu, Zhipeng Liu, Lin Fang, Zhiling Liu, Yuhuan Xie, Melissa M. Hudson, Shanaya Rathod, David Kingdon, Nusrat Husain, Xudong Liu, Muhammad Ayub, Farooq Naeem

    Vydáno 2017
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  14. 14
    Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation

    Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation Autor Asif Mir, Liana Kaufman, Abdul Noor, M. Mahdi Motazacker, Talal Jamil, Matloob Azam, Kimia Kahrizi, Muhammad Rafiq, Rosanna Weksberg, Tanveer Nasr, Farooq Naeem, Andreas Tzschach, Andreas W. Kuß, Gisele E. Ishak, Dan Doherty, Hans‐Hilger Ropers, A. James Barkovich, Hossein Najmabadi, Muhammad Ayub, John B. Vincent

    Vydáno 2009
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  15. 15
    Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability

    Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability Autor Taimoor I. Sheikh, Nasim Vasli, Stephen F. Pastore, Kimia Kharizi, Ricardo Harripaul, Zohreh Fattahi, Shruti Pande, Farooq Naeem, A. Hussain, Asif Mir, Omar Islam, Katta M. Girisha, Muhammad Irfan, Muhammad Ayub, Christoph Schwarzer, Hossein Najmabadi, Anju Shukla, Valentina C. Sladky, Vincent Z. Braun, Irmina García-Carpio, Andreas Villunger, John B. Vincent

    Vydáno 2021
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  16. 16
    Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

    Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability Autor Muhammad Rafiq, Andreas W. Kuß, Lucia Puettmann, Abdul Noor, Annapoorani Ramiah, Ghazanfar Ali, Hao Hu, Nadir Ali Kerio, Yong Xiang, Masoud Garshasbi, Muzammil Ahmad Khan, Gisele E. Ishak, Rosanna Weksberg, Reinhard Ullmann, Andreas Tzschach, Kimia Kahrizi, Khalid Mahmood, Farooq Naeem, Muhammad Ayub, Kelley W. Moremen, John B. Vincent, Hans Hilger Ropers, Muhammad Ansar, Hossein Najmabadi

    Vydáno 2011
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  17. 17
    Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

    Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families Autor Ricardo Harripaul, Nasim Vasli, А. О. Михайлов, Muhammad Rafiq, Kirti Mittal, Christian Windpassinger, Taimoor I. Sheikh, Abdul Noor, Hina Mahmood, Samantha I Downey, Maneesha Johnson, Kayla Vleuten, Lauren Bell, Muhammad Ilyas, Falak Sher Khan, Valeed Khan, Mohammad Moradi, M. Ayaz, Farooq Naeem, Asieh Heidari, Iqra I. Ahmed, Shirin Ghadami, Zehra Agha, Sirous Zeinali, Raheel Qamar, Hossein Mozhdehipanah, Peter John, Asif Mir, Muhammad Ansar, Leon French, Muhammad Ayub, John B. Vincent

    Vydáno 2017
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  18. 18
    Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

    Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations Autor Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, Henry S. Aghanwa, Moin Ahmad Ansari, Aftab Asif, Rubina Aslam, José Luis Ayuso, Tim B. Bigdeli, Stefano Bignotti, Julio Bobes, Bekh Bradley, P.F. Buckley, Murray J. Cairns, Stanley V. Catts, Abdul Rashid Chaudhry, David Cohen, Brett Collins, Angèle Consoli, Javier Costas, Benedicto Crespo‐Facorro, Nikolaos P. Daskalakis, Michael Davidson, Kenneth L. Davis, Faith Dickerson, Imtiaz Ahmad Dogar, Elodie Drapeau, Lourdes Fañanás, Ayman H. Fanous, Warda Fatima, Mar Fatjó‐Vilas, Cheryl Filippich, Joseph I. Friedman, John F. Fullard, Penelope Georgakopoulos, Marianna Giannitelli, Ina Giegling, Melissa J. Green, Olivier Guillin, Blanca Gutiérrez, Herlina Y. Handoko, Stella Kim Hansen, Maryam Haroon, Vahram Haroutunian, Frans Henskens, Fahad Hussain, Assen Jablensky, Jamil Junejo, Brian Kelly, Shams-ud-Din Ahmad Khan, Muhammad Nasar Sayeed Khan, Anisuzzaman Khan, Hamid R. Khawaja, Bakht Khizar, Steven P. Kleopoulos, James A. Knowles, Bettina Konte, Agung Kusumawardhani, Naeemullah Leghari, Xudong Liu, Adriana Lori, Carmel M. Loughland, Khalid Mahmood, Saqib Mahmood, Dolores Malaspina, Danish J. Malik, Amy J. M. McNaughton, Patricia T. Michie, Vasiliki Michopolous, Esther Molina, María Dolores Moltó, Asim Munir, Gerard Muntané, Farooq Naeem, Derek J. Nancarrow, Amina Nasar, Tanvir Nasr, Jude U. Ohaeri, Jürg Ott, Christos Pantelis, Sathish Periyasamy, Ana González‐Pinto, Abigail Powers, Belén Ramos, Nusrat Habib Rana, Mark Hyman Rapaport, Abraham Reichenberg

    Vydáno 2023
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