A. Eran

发表

J. Aharon-Peretz, T. Siman-Tov, E. Sprecher, 2017, Front. Aging Neurosci..

COG6‐CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex development

H. Mandel, Y. Goldberg, L. Kalfon, 2020, Clinical genetics.

Ischemic Stroke, Aortic Dissection, and Thrombolytic Therapy—the Importance of Basic Clinical Skills

A. Eran, M. Grupper, A. Shifrin, 2007, Journal of General Internal Medicine.

Mechanism underlying painful radiculopathy in patients with lumbar disc herniation

E. Eisenberg, A. Eran, G. Sviri, 2022, European journal of pain.

Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review

H. Mandel, S. Ravid, Ann Saada, 2019, Metabolic Brain Disease.

Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

D. Behar, H. Mandel, D. Goldsher, 2015, Human Genetics.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

D. Behar, H. Mandel, D. Goldsher, 2014, Human Genetics.

A novel homozygous splice site mutation in NALCN identified in siblings with cachexia, strabismus, severe intellectual disability, epilepsy and abnormal respiratory rhythm.

H. Mandel, E. Levanon, D. Magen, 2016, European journal of medical genetics.

Perineural Spread in Noncutaneous Head and Neck Cancer: New Insights into an Old Problem

S. Billan, M. Amit, Z. Gil, 2016, Journal of Neurological Surgery—Part B.

Unusual Case of Leptomeningeal Dissemination of a Diffuse Pontine High-Grade Astrocytoma in a Child

S. Postovsky, A. Eran, M. Weyl Ben Arush, 2008, Pediatric Neurosurgery.

Two separate functions of NME3 critical for cell survival underlie a neurodegenerative disorder

J. Liao, H. Mandel, S. Hsieh, 2018, Proceedings of the National Academy of Sciences.

5th International Symposium on Focused Ultrasound

Matthew E. Downs, Gregory T. Clement, Chang Kyu Park, 2016, Journal of Therapeutic Ultrasound.

Microemboli in MCA ipsilateral to occluded common carotid artery: an observation and short review of the literature

D. Yarnitsky, D. Goldsher, A. Eran, 2008, Neurological research.

Posterior reversible encephalopathy syndrome after combined general and spinal anesthesia with intrathecal morphine.

M. Barak, A. Eran, 2009, Anesthesia and analgesia.

Torticollis in children - differential diagnosis approach

A. Eran, 2015 .

CT multiplanar reconstructions (MPR) for shrapnel injury trajectory

A. Engel, A. Eran, O. Brook, 2011, Emergency Radiology.

Recurrent opportunistic infections in a post-transplant lymphoma patient

I. Avivi, A. Eran, K. Hussein, 2012 .

Bariatric Surgery-Associated Myelopathy

S. Ravid, A. Eran, R. Weiss, 2021, Obesity Facts.

Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course.

F. Benfenati, H. Mandel, E. Levanon, 2019, Brain : a journal of neurology.

EPT1 (selenoprotein I) is critical for the neural development and maintenance of plasmalogen in humans[S]

H. Mandel, Y. Hirabayashi, H. Sugimoto, 2018, Journal of Lipid Research.

Fluoroscopically Guided Cervical Inter-Laminar Epidural Injections: Correlation Between Degree of Spinal Stenosis and Contrast Dispersal Pattern

Y. Safriel, A. Eran, A. Haboosheh, 2016 .

Metastatic Rhabdoid Meningioma with BRAF V600E Mutation and Good Response to Personalized Therapy: Case Report and Review of the Literature

S. Postovsky, E. Vlodavsky, S. Constantini, 2015, Pediatric hematology and oncology.

Tectorial Membrane Injury: Frequently Overlooked in Pediatric Traumatic Head Injury

T. Huisman, A. Tekes, A. Poretti, 2011, American Journal of Neuroradiology.

Asymmetry of the Odontoid Lateral Mass Interval in Pediatric Trauma CT: Do We Need to Investigate Further?

D. Yousem, I. Izbudak, A. Eran, 2016, American Journal of Neuroradiology.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

D. Behar, H. Mandel, D. Goldsher, 2014, Human Genetics.

Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variants

H. Mandel, L. Kalfon, T. Falik-Zaccai, 2021, Molecular genetics & genomic medicine.

Medulloblastoma: atypical CT and MRI findings in children

I. Izbudak, N. Aygun, A. Ozturk, 2010, Pediatric Radiology.

Suspected CNS Metastases of Askin's Tumor: Would You Irradiate the Neural Axis?

A. Kuten, G. Bar-Sela, O. Kaidar-Person, 2012, World journal of oncology.

Survival impact of the time gap between surgery and chemo-radiotherapy in Glioblastoma patients

O. Kaidar-Person, A. Eran, T. Tzuk-Shina, 2020, Scientific Reports.

Orbital Fissures