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Items: 1 to 20 of 48

1.

Error occurred: cannot get document summary

PMID:
24250758

2.

Family Focused Care for Refugees and Displaced Populations: Global Opportunities for Family Therapists.

Patterson JE, Abu-Hassan HH, Vakili S, King A.

J Marital Fam Ther. 2017 Dec 1. doi: 10.1111/jmft.12295. [Epub ahead of print]

PMID:
29194696
3.

Tailoring the Oxygen Reduction Activity of Hemoglobin through Immobilization within Microporous Organic Polymer-Graphene Composite.

Soliman AB, Haikal RR, Abugable AA, Hassan MH, Karakalos SG, Pellechia PJ, Hassan HH, Yacoub MH, Alkordi MH.

ACS Appl Mater Interfaces. 2017 Aug 23;9(33):27918-27926. doi: 10.1021/acsami.7b06146. Epub 2017 Jun 27.

PMID:
28621530
4.

Assessment of the cochlear nerve to facial nerve size ratio using MR multiplanar reconstruction of the internal auditory canal in patients presenting with acquired long-standing hearing loss.

Naguib NNN, Hey C, Shaaban MS, Elabd AM, Hassan HHM, Gruber-Rouh T, Kaltenbach B, Harth M, Ackermann H, Stöver T, Vogl TJ, Nour-Eldin NA.

Br J Radiol. 2017 May;90(1073):20160870. doi: 10.1259/bjr.20160870. Epub 2017 Apr 3.

PMID:
28368665
5.

Idiopathic intracranial hypertension in children: Diagnostic and management approach.

Albakr A, Hamad MH, Alwadei AH, Bashiri FA, Hassan HH, Idris H, Hassan S, Muayqil T, Altweijri I, Salih MA.

Sudan J Paediatr. 2016;16(2):67-76.

6.

Modified MR defecography without rectal filling in obstructed defecation syndrome: Initial experience.

Hassan HH, Elnekiedy AM, Elshazly WG, Naguib NN.

Eur J Radiol. 2016 Sep;85(9):1673-81. doi: 10.1016/j.ejrad.2016.06.014. Epub 2016 Jun 24.

PMID:
27501905
7.

A 12-gene signature to distinguish colon cancer patients with better clinical outcome following treatment with 5-fluorouracil or FOLFIRI.

Paquet ER, Cui J, Davidson D, Pietrosemoli N, Hassan HH, Tsofack SP, Maltais A, Hallett MT, Delorenzi M, Batist G, Aloyz R, Lebel M.

J Pathol Clin Res. 2015 Apr 9;1(3):160-72. doi: 10.1002/cjp2.17. eCollection 2015 Jul.

8.

Surface functionality and electrochemical investigations of a graphitic electrode as a candidate for alkaline energy conversion and storage devices.

Soliman AB, Abdel-Samad HS, Abdel Rehim SS, Hassan HH.

Sci Rep. 2016 Feb 26;6:22056. doi: 10.1038/srep22056.

9.

Glutaric aciduria type 1 as a cause of dystonic cerebral palsy.

Mohamed S, Hamad MH, Hassan HH, Salih MA.

Saudi Med J. 2015 Nov;36(11):1354-7. doi: 10.15537/smj.2015.11.12132.

10.

Synthesis and biological evaluation of new nanosized aromatic polyamides containing amido- and sulfonamidopyrimidines pendant structures.

Hassan HH, Mansour EM, Abou Zeid AM, El-Helow ER, Elhusseiny AF, Soliman R.

Chem Cent J. 2015 Aug 19;9:44. doi: 10.1186/s13065-015-0123-2. eCollection 2015.

11.

Two complementary approaches for intracellular delivery of exogenous enzymes.

Rust A, Hassan HH, Sedelnikova S, Niranjan D, Hautbergue G, Abbas SA, Partridge L, Rice D, Binz T, Davletov B.

Sci Rep. 2015 Jul 24;5:12444. doi: 10.1038/srep12444.

12.

Agenesis of the corpus callosum associated with spinal open neural tube defect.

Elgamal EA, Elwatidy SM, Alhabib AF, Jamjoom ZB, Murshid WR, Hassan HH, Salih MA.

Saudi Med J. 2014 Dec;35 Suppl 1:S57-63.

13.

Split cord malformation associated with spinal open neural tube defect.

Elgamal EA, Hassan HH, Elwatidy SM, Altwijri I, Alhabib AF, Jamjoom ZB, Murshid WR, Salih MA.

Saudi Med J. 2014 Dec;35 Suppl 1:S44-8.

14.

Sturge-Weber syndrome: Continued vigilance is needed.

Hassan S, Babiker A, Bashiri FA, Hassan HH, Husseini ME, Salih MA.

Sudan J Paediatr. 2015;15(2):63-70.

15.

Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulation.

Khan AO, AlDrees A, Elmalik SA, Hassan HH, Michel M, Stevanin G, Azzedine H, Salih MA.

Br J Ophthalmol. 2014 Jul;98(7):889-93.

PMID:
24522175
16.

The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.

Kentab AY, Hassan HH, Hamad MH, Alhumidi A.

Sudan J Paediatr. 2014;14(2):61-70.

17.

Pellagra-like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit.

Hijazi H, Salih MA, Hamad MH, Hassan HH, Salih SB, Mohamed KA, Mukhtar MM, Karrar ZA, Ansari S, Ibrahim N, Alkuraya FS.

Clin Genet. 2015;87(1):56-61. doi: 10.1111/cge.12325. Epub 2013 Dec 20.

PMID:
24354460
18.

New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.

Salih MA, Mundwiller E, Khan AO, AlDrees A, Elmalik SA, Hassan HH, Al-Owain M, Alkhalidi HM, Katona I, Kabiraj MM, Chrast R, Kentab AY, Alzaidan H, Rodenburg RJ, Bosley TM, Weis J, Koenig M, Stevanin G, Azzedine H.

PLoS One. 2013 Oct 9;8(10):e76831. doi: 10.1371/journal.pone.0076831. eCollection 2013. Erratum in: PLoS One. 2013;8(11). doi:10.1371/annotation/cb01a74a-3330-4412-8040-2a94842420ed.

19.

A newly recognized autosomal recessive syndrome affecting neurologic function and vision.

Salih MA, Tzschach A, Oystreck DT, Hassan HH, AlDrees A, Elmalik SA, El Khashab HY, Wienker TF, Abu-Amero KK, Bosley TM.

Am J Med Genet A. 2013 Jun;161A(6):1207-13. doi: 10.1002/ajmg.a.35850. Epub 2013 Apr 30.

PMID:
23633300
20.

NPHP4 mutation is linked to cerebello-oculo-renal syndrome and male infertility.

Alazami AM, Alshammari MJ, Baig M, Salih MA, Hassan HH, Alkuraya FS.

Clin Genet. 2014 Apr;85(4):371-5. doi: 10.1111/cge.12160. Epub 2013 Apr 26.

PMID:
23574405

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