Abdulkareem, Imran: search on Z-Library

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1

Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability

Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Pushparaj, Peter Natesan, Bibi, Fehmida, Chaudhary, Adeel G.

Journal:

Frontiers in Genetics

Year:

2020

File:

PDF, 821 KB

2020

2

Effects of Indomethacin on Expression of Pten Tumor Suppressor in Human Cancers

Imran Haruna Abdulkareem, Maria Blair

Journal:

International Journal of Surgery

Year:

2010

Language:

english

File:

PDF, 112 KB

english, 2010

3

Systematic review of clinical effectiveness of allopurinol in treating gout, compared to febuxostat, AMONG patients with confirmed diagnosis of gout

Ibrahim Bala Zurmi, Imran Haruna Abdulkareem, C. Carroll

Journal:

International Journal of Surgery

Year:

2011

Language:

english

File:

PDF, 50 KB

english, 2011

4

A systematic review of treatment of acromiclavicular joint (ACJ) injuries

Abdulkareem, Imran Haruna

Journal:

International Journal of Surgery

Year:

2012

Language:

english

File:

PDF, 46 KB

english, 2012

5

The use of non-orthopaedic devices for orthopaedic procedures

George, Akintunde, Abdulkareem, Imran, Bould, Michael, Spencer, Robert

Journal:

Year:

2013

Language:

english

File:

PDF, 103 KB

english, 2013

6

Cytotoxicity and genotoxicity of gliotoxin on human lymphocytes in vitro

Nouri, Mohammed Adel, Al-Halbosiy, Mohammed M.F., Dheeb, Batol Imran, Hashim, Abdulkareem Jasim

Journal:

Journal of King Saud University - Science

Year:

2015

Language:

english

File:

PDF, 985 KB

english, 2015

7

Molecular identification of clinical Candida isolates by simple and randomly amplified polymorphic DNA-PCR

Al-Tekreeti, Afnan R. A., Al-Halbosiy, Mohammad M. F., Dheeb, Batol Imran, Hashim, Abdulkareem Jasim, Al-Zuhairi, Anaam Fuad Hussain, Mohammad, Farooq Ibrahem

Journal:

Arabian Journal for Science and Engineering

Year:

2017

Language:

english

File:

PDF, 1.04 MB

english, 2017

8

A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy

Naseer, Muhammad Imran, Alwasiyah, Mohammad Khalid, Abdulkareem, Angham Abdulrahman, Bajammal, Rayan Abdullah, Trujillo, Carlos, Abu-Elmagd, Muhammad, Jafri, Mohammad Alam, Chaudhary, Adeel G., Al-Qah

Journal:

Genes & Genomics

Year:

2018

Language:

english

File:

PDF, 1012 KB

english, 2018

9

A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family

Abdulkareem, Angham Abdulrahman, Abulnaja, Khalid Omar, Jan, Mohammad M., Karim, Sajjad, Rasool, Mahmood, Ansari, Shakeel Ahmed, Chaudhary, Adeel G., Al-Qahtani, Mohammad H., Naseer, Muhammad Imran

Journal:

Neurological Sciences

Year:

2018

Language:

english

File:

PDF, 761 KB

english, 2018

10

Reactivity of commercially available monoclonal antibodies to human CD antigens with peripheral blood leucocytes of dromedary camels (Camelus dromedarius)

Hussen, Jamal, Shawaf, Turke, Al-herz, Abdulkareem Imran, Alturaifi, Hussain R., Alluwaimi, Ahmed M.

Journal:

Open Veterinary Journal

Year:

2017

Language:

english

File:

PDF, 726 KB

english, 2017

11

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

12

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

13

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

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

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

16

Histopathological changes and expression of transforming growth factor beta (TGF-β3) in mice exposed to gliotoxin

Hussain, Anaam Fuad, Sulaiman, Ghassan Mohammad, Dheeb, Batol Imran, Hashim, Abdulkareem Jasim, Alrahman, Eman Sabah Abd, Seddiq, Sara Haitham, Khashman, Basim M.

Journal:

Journal of King Saud University - Science

Year:

2018

File:

PDF, 3.35 MB

2018

17

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

18

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

19

Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis

Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, GuzmÃ¡n-Vega, Francisco J., Arold, Stefan T., Pushparaj, Peter Natesan, Chaudhary, Adeel G., AlQahtani, Mohammad H.

Journal:

Frontiers in Genetics

Year:

2020

File:

PDF, 1.14 MB

2020

20

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

21

Association of overweight/obesity with the severity of periodontitis using BPE code in an iraqi population

Gul, Sarhang S., Imran, Nada K., Al-Sharqi, Ali JB., Abdulkareem, Ali A.

Journal:

Clinical Epidemiology and Global Health

Year:

2020

File:

PDF, 508 KB

2020

22

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