Algahtani, Mohammad: search on Z-Library

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1

Cultural adaptation of cognitive behavioural therapy (CBT) for patients with depression and anxiety in Saudi Arabia and Bahrain: a qualitative study exploring views of patients, carers, and mental health professionals

Algahtani, Haifa Mohammad Saleh, Almulhim, Abdullah, AlNajjar, Fatema Ali, Ali, Mazen Khalil, Irfan, Muhammad, Ayub, Muhammad, Naeem, Farooq

Journal:

The Cognitive Behaviour Therapist

Year:

2019

Language:

english

File:

PDF, 294 KB

english, 2019

2

Regulation of cell cycle by MDM2 in prostate cancer cells through Aurora Kinase-B and p21WAF1/CIP1 mediated pathways

Kanagasabai, Thanigaivelan, Venkatesan, Thiagarajan, Natarajan, Umamaheswari, Alobid, Saad, Alhazzani, Khalid, Algahtani, Mohammad, Rathinavelu, Appu

Journal:

Cellular Signalling

Year:

2020

Language:

english

File:

PDF, 3.86 MB

english, 2020

3

Evaluation of date seed (Phoenix dactylifera L.) oil as crop base stock for environment friendly industrial lubricants

Ahmed, Mohammed Shabbir, Nair, K. Prabhakaran, Khan, Mohammed Sadique, Algahtani, Ali, Rehan, Mohammad

Journal:

Biomass Conversion and Biorefinery

Year:

2020

File:

PDF, 605 KB

2020

4

[IEEE 2014 IEEE 29th International Conference on Microelectronics (MIEL) - Belgrade, Serbia (2014.5.12-2014.5.14)] 2014 29th International Conference on Microelectronics Proceedings - MIEL 2014 - Low temperature of formation of nickel germanide on crystalline germanium

Algahtani, Fahid, Blackford, Mark, Alnassar, Mohammad Saleh N, Reeves, Geoffrey K., Leech, Patrick, Pirogova, Elena, Holland, Anthony S.

Year:

2014

Language:

english

File:

PDF, 585 KB

english, 2014

5

Nanoemulsion loaded polymeric hydrogel for Topical delivery of curcumin in Psoriasis

Algahtani, Mohammed S., Ahmad, Mohammad Zaki, Ahmad, Javed

Journal:

Journal of Drug Delivery Science and Technology

Year:

2020

File:

PDF, 11.77 MB

2020

6

A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Algahtani, Hussein, Shirah, Bader, Alharbi, Suzan Y., Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Journal of Stroke and Cerebrovascular Diseases

Year:

2020

File:

PDF, 958 KB

2020

7

Molecular genetics of human primary microcephaly: an overview

Faheem, Muhammad, Naseer, Muhammad Imran, Rasool, Mahmood, Chaudhary, Adeel G, Kumosani, Taha A, Ilyas, Asad Muhammad, Pushparaj, Peter, Ahmed, Farid, Algahtani, Hussain A, Al-Qahtani, Mohammad H, Sal

Journal:

BMC Medical Genomics

Year:

2015

Language:

english

File:

PDF, 517 KB

english, 2015

8

A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia

Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

International Journal of Neuroscience

Year:

2020

Language:

english

File:

PDF, 1.63 MB

english, 2020

9

Role of rivaroxaban in sunitinib-induced renal injuries via inhibition of oxidative stress-induced apoptosis and inflammation through the tissue nacrosis factor-Î± induced nuclear factor-Îºappa B signaling pathway in rats

Al-Harbi, Naif O., Imam, Faisal, Alharbi, Mohammad Matar, Khan, Mohammad Rashid, Qamar, Wajhul, Afzal, Muhammad, Algahtani, Mohammad, Alobaid, Saad, Alfardan, Ali Salim, Alshammari, Abdulrahman, Albek

Journal:

Journal of Thrombosis and Thrombolysis

Year:

2020

File:

PDF, 1.40 MB

2020

10

Nanoemulgel for Improved Topical Delivery of Retinyl Palmitate: Formulation Design and Stability Evaluation

Algahtani, Mohammed S., Ahmad, Mohammad Zaki, Ahmad, Javed

Journal:

Year:

2020

File:

PDF, 4.03 MB

2020

11

A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine

Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Intractable & Rare Diseases Research

Year:

2019

Language:

english

File:

PDF, 752 KB

english, 2019

12

[IEEE SoutheastCon 2017 - Concord, NC, USA (2017.3.30-2017.4.2)] SoutheastCon 2017 - Circular Cross Kelvin Resistor test structure for low specific contact resistivity

Luong, Stanley, Alnassar, Mohammad Saleh N., Yue, Pan, Holland, Anthony S., Algahtani, Fahid

Year:

2017

Language:

english

File:

PDF, 247 KB

english, 2017

13

Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient

Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Naseer, Muhammad Imran, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman

Journal:

Intractable & Rare Diseases Research

Year:

2018

Language:

english

File:

PDF, 1.53 MB

english, 2018

14

A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene

Algahtani, Hussein, Al-Hakami, Fahad, Al-Shehri, Mohammed, Shirah, Bader, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Year:

2019

File:

PDF, 2.83 MB

2019

15

Multinational comparative cross-sectional survey of views of medical students about acceptable terminology and subgroups in schizophrenia

Rathod, Shanaya, Irfan, Muhammad, Bhargava, Rachna, Pinninti, Narsimha, Scott, Joseph, Mohammad Algahtani, Haifa, Guo, Zhihua, Gupta, Rishab, Nadkarni, Pallavi, Naeem, Farooq, Howells, Fleur, Sorsdahi

Journal:

Year:

2018

Language:

english

File:

PDF, 745 KB

english, 2018

16

Investigation Utilizing the HLB Concept for the Development of Moisturizing Cream and Lotion: In-Vitro Characterization and Stability Evaluation

Alam, Shoaib, Algahtani, Mohammed S., Ahmad, Mohammad Zaki, Ahmad, Javed

Journal:

Year:

2020

File:

PDF, 1.75 MB

2020

17

On the calibration and applicability of global solar radiation models based on temperature extremities in India

Jamil, Basharat, Irshad, Kashif, Algahtani, Ali, Islam, Saiful, Ali, Mohammad A., Shahab, Azam

Journal:

Environmental Progress & Sustainable Energy

Year:

2019

Language:

english

File:

PDF, 1.43 MB

english, 2019

18

Co-Delivery of Imiquimod and Curcumin by Nanoemugel for Improved Topical Delivery and Reduced Psoriasis-Like Skin Lesions

Algahtani, Mohammed S., Ahmad, Mohammad Zaki, Nourein, Ihab Hamed, Ahmad, Javed

Journal:

Year:

2020

File:

PDF, 3.97 MB

2020

19

Novel strategies for assessing platelet reactivity

Algahtani, Mohammad, Heptinstall, Stan

Journal:

Future Cardiology

Year:

2017

Language:

english

File:

PDF, 1.76 MB

english, 2017

20

A novel mutation in TTN gene in a Saudi patient with bilateral facial weakness and scapular winging

Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Intractable & Rare Diseases Research

Year:

2019

File:

PDF, 539 KB

2019

21

Case report with review of literature for the dilemma of diagnosis of CLIPPERS

Ramadan, Shadi M, Al-Ghamdi, Abdulaziz, Saleh, A Idris, Muddassir, Rabia, Rahman, Sayed S, Attahan, Ayman, Algahtani, Mohammad, Ghaith, Mazen M, Theyab, Abdulrahman

Journal:

Future Neurology

Year:

2019

File:

PDF, 4.33 MB

2019

22

Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family

Algahtani, Hussein, Naseer, Muhammad Imran, Al-Qahtani, Mohammad, Abdulrahman, Shireen Abubakr, Boker, Faisal, Shirah, Bader

Journal:

Journal of the Neurological Sciences

Year:

2016

Language:

english

File:

PDF, 773 KB

english, 2016

23

Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family

Algahtani, Hussein, Shirah, Bader, Ullah, Ikram, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Genes & Diseases

Year:

2019

Language:

english

File:

PDF, 1.03 MB

english, 2019

24

A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene

Algahtani, Hussein, Al-Hakami, Fahad, Al-Shehri, Mohammed, Shirah, Bader, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Year:

2019

Language:

english

File:

PDF, 2.83 MB

english, 2019

25

A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17

Algahtani, Hussein, Shirah, Bader, Almatrafi, Samah, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

Journal:

Neurological Research

Year:

2020

File:

PDF, 1.97 MB

2020

26

Possible Role of Kaempferol in Reversing Oxidative Damage, Inflammation, and Apoptosis-Mediated Cortical Injury Following Cadmium Exposure

Al-Brakati, Ashraf, Albarakati, Alaa Jameel A., Lokman, Maha S., Theyab, Abdulrahman, Algahtani, Mohammad, Menshawi, Salah, AlAmri, Ohoud D., Al omairi, Naif E., Essawy, Ehab A., Kassab, Rami B., Abde

Journal:

Neurotoxicity Research

Year:

2020

File:

PDF, 1.34 MB

2020

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