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Items: 1 to 20 of 402

  • The following term was not found in PubMed: Mohamadi-Ivatloo.
1.

The investigation of relevancy between PIAS1 and PIAS2 gene expression and disease severity of multiple sclerosis.

Kouchaki E, Nikoueinejad H, Akbari H, Azimi S, Behnam M.

J Immunoassay Immunochem. 2019 May 13:1-11. doi: 10.1080/15321819.2019.1613244. [Epub ahead of print]

PMID:
31084243
2.

Not All Shock Is Created Equal: Developing a Standardized Treatment Approach for Cardiogenic Shock.

Tehrani BN, Rosner C, Sinha SS.

JACC Heart Fail. 2019 May 3. pii: S2213-1779(19)30096-4. doi: 10.1016/j.jchf.2019.01.014. [Epub ahead of print] No abstract available.

PMID:
31078478
3.

Reconstruction of sternoclavicular defect with completely detached pectoralis major flap.

Opoku-Agyeman J, Perez S, Behnam A, Matera D.

J Surg Case Rep. 2019 Apr 24;2019(4):rjz122. doi: 10.1093/jscr/rjz122. eCollection 2019 Apr.

4.

Therapeutic Application of Micellar Solubilized Xanthohumol in a Western-Type Diet-Induced Mouse Model of Obesity, Diabetes and Non-Alcoholic Fatty Liver Disease.

Mahli A, Seitz T, Freese K, Frank J, Weiskirchen R, Abdel-Tawab M, Behnam D, Hellerbrand C.

Cells. 2019 Apr 17;8(4). pii: E359. doi: 10.3390/cells8040359.

5.

IgG4-related disease: Association with a rare gene variant expressed in cytotoxic T cells.

Newman JH, Shaver A, Sheehan JH, Mallal S, Stone JH, Pillai S, Bastarache L, Riebau D, Allard-Chamard H, Stone WM, Perugino C, Pilkinton M, Smith SA, McDonnell WJ, Capra JA, Meiler J, Cogan J, Xing K, Mahajan VS, Mattoo H, Hamid R, Phillips JA 3rd; Undiagnosed Disease Network.

Mol Genet Genomic Med. 2019 Apr 16:e686. doi: 10.1002/mgg3.686. [Epub ahead of print]

6.

Predictors of chemotherapy-induced severe anemia in cancer patients receiving chemotherapy.

Razzaghdoust A, Mofid B, Peyghambarlou P.

Support Care Cancer. 2019 Apr 16. doi: 10.1007/s00520-019-04780-7. [Epub ahead of print]

PMID:
30993448
7.

An optimized isolation protocol yields high-quality RNA from cassava tissues (Manihot esculenta Crantz).

Behnam B, Bohorquez-Chaux A, Castaneda-Mendez OF, Tsuji H, Ishitani M, Becerra Lopez-Lavalle LA.

FEBS Open Bio. 2019 Feb 20;9(4):814-825. doi: 10.1002/2211-5463.12561. eCollection 2019 Apr.

8.

High-Intensity Focused Ultrasound Lesion Detection Using Adaptive Compressive Sensing Based on Empirical Mode Decomposition.

Ghasemifard H, Behnam H, Tavakkoli J.

J Med Signals Sens. 2019 Jan-Mar;9(1):24-32. doi: 10.4103/jmss.JMSS_17_18.

9.

A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.

Zastrow DB, Kohler JN, Bonner D, Reuter CM, Fernandez L, Grove ME, Fisk DG; Undiagnosed Diseases Network, Yang Y, Eng CM, Ward PA, Bick D, Worthey EA, Fisher PG, Ashley EA, Bernstein JA, Wheeler MT 3rd.

J Genet Couns. 2019 Apr;28(2):213-228. doi: 10.1002/jgc4.1119. Erratum in: J Genet Couns. 2019 May 21;:.

PMID:
30964584
10.

Standardized Team-Based Care for Cardiogenic Shock.

Tehrani BN, Truesdell AG, Sherwood MW, Desai S, Tran HA, Epps KC, Singh R, Psotka M, Shah P, Cooper LB, Rosner C, Raja A, Barnett SD, Saulino P, deFilippi CR, Gurbel PA, Murphy CE, O'Connor CM.

J Am Coll Cardiol. 2019 Apr 9;73(13):1659-1669. doi: 10.1016/j.jacc.2018.12.084.

11.

Carbon nanomaterials and amyloid-beta interactions: potentials for the detection and treatment of Alzheimer's disease?

Mohajeri M, Behnam B, Barreto GE, Sahebkar A.

Pharmacol Res. 2019 May;143:186-203. doi: 10.1016/j.phrs.2019.03.023. Epub 2019 Mar 31. Review.

PMID:
30943430
12.

Genetics and genomic medicine in Iran.

Behnam B, Zakeri M.

Mol Genet Genomic Med. 2019 Feb;7(2):e00606. doi: 10.1002/mgg3.606.

13.

Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.

Burrage LC, Reynolds JJ, Baratang NV, Phillips JB, Wegner J, McFarquhar A, Higgs MR, Christiansen AE, Lanza DG, Seavitt JR, Jain M, Li X, Parry DA, Raman V, Chitayat D, Chinn IK, Bertuch AA, Karaviti L, Schlesinger AE, Earl D, Bamshad M, Savarirayan R, Doddapaneni H, Muzny D, Jhangiani SN, Eng CM, Gibbs RA, Bi W, Emrick L, Rosenfeld JA, Postlethwait J, Westerfield M, Dickinson ME, Beaudet AL, Ranza E, Huber C, Cormier-Daire V, Shen W, Mao R, Heaney JD, Orange JS; University of Washington Center for Mendelian Genomics; Undiagnosed Diseases Network, Bertola D, Yamamoto GL, Baratela WAR, Butler MG, Ali A, Adeli M, Cohn DH, Krakow D, Jackson AP, Lees M, Offiah AC, Carlston CM, Carey JC, Stewart GS, Bacino CA, Campeau PM, Lee B.

Am J Hum Genet. 2019 Mar 7;104(3):422-438. doi: 10.1016/j.ajhg.2019.01.007. Epub 2019 Feb 14.

14.

Optimization of a raceway pond system for wastewater treatment: a review.

Rayen F, Behnam T, Dominique P.

Crit Rev Biotechnol. 2019 May;39(3):422-435. doi: 10.1080/07388551.2019.1571007. Epub 2019 Feb 11.

PMID:
30744439
15.

Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.

Grove ME, White S, Fisk DG, Rego S, Dagan-Rosenfeld O, Kohler JN, Reuter CM, Bonner D; Undiagnosed Diseases Network, Wheeler MT, Bernstein JA, Ormond KE, Hanson-Kahn AK.

J Genet Couns. 2019 Apr;28(2):466-476. doi: 10.1002/jgc4.1094. Epub 2019 Feb 1.

PMID:
30706981
16.

Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.

Kelly M, Park M, Mihalek I, Rochtus A, Gramm M, PĂ©rez-Palma E, Axeen ET, Hung CY, Olson H, Swanson L, Anselm I, Briere LC, High FA, Sweetser DA; Undiagnosed Diseases Network, Kayani S, Snyder M, Calvert S, Scheffer IE, Yang E, Waugh JL, Lal D, Bodamer O, Poduri A.

Epilepsia. 2019 Mar;60(3):406-418. doi: 10.1111/epi.14653. Epub 2019 Jan 25.

PMID:
30682224
17.

Cognitive functions and white matter lesions on magnetic resonance images in a sample of normal Iranian population with cardiovascular risk factors.

Ashrafi F, Taheri MS, Farzaneh A, Behnam B, Ahmadi MA.

Neuroradiol J. 2019 Apr;32(2):108-114. doi: 10.1177/1971400919825862. Epub 2019 Jan 24.

PMID:
30674224
18.

Skull's Photoacoustic Attenuation and Dispersion Modeling with Deterministic Ray-Tracing: Towards Real-Time Aberration Correction.

Mohammadi L, Behnam H, Tavakkoli J, Avanaki MRN.

Sensors (Basel). 2019 Jan 16;19(2). pii: E345. doi: 10.3390/s19020345.

20.

C3 Glomerulonephritis With Multiple Mutations in Complement Factor H.

Dalili N, Behnam B, Vali F, Parvin M, Torbati P, Rasaii N, Samadian F, Ahmadpoor P.

Iran J Kidney Dis. 2018 Nov;12(6):376-381.

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