Clinical Spectrum of Cerebral Palsy and Associated Disability in South Egypt: A Local Survey Study

por Abas, Osama, Abdelaziem, Faten, Kilany, Ayman
Publicado 2017

Acute Aortic Occlusion Presenting as Flaccid Paraplegia

por Kilany, Ayman, Al-Hashel, Jasem Y., Rady, Azza
Publicado 2015

Opsoclonus myoclonus ataxia syndrome following COVID-19 infection

por Ismail, Ismail Ibrahim, Kamel, Walaa A., Kilany, Ayman
Publicado 2022

Parkinsonism as a Complication of Bariatric Surgery

por Kamel, Walaa A., Hashel, Jasem Y. Al, Kilany, Ayman, Altailji, Samira
Publicado 2015

Whole exome screening of neurodevelopmental regression disorders in a cohort of Egyptian patients

por Refeat, Miral M., Naggar, Walaa El, Saied, Mostafa M. El, Kilany, Ayman
Publicado 2022

Variable predicted pathogenic mechanisms for novel MECP2 variants in RTT patients

por Sharaf-Eldin, Wessam E., Issa, Mahmoud Y., Zaki, Maha S., Kilany, Ayman, Fayez, Alaaeldin G.
Publicado 2022

Association analysis of genetic variations of eNOS and α(2)β(1) integrin genes with type 2 diabetic retinopathy

por Azmy, Rania, Dawood, Ashraf, Kilany, Ayman, El-Ghobashy, Yasser, Ellakwa, Amin Faisal, El-Daly, May
Publicado 2012

The Role of Double Modality Ultrasonographic and Fluoroscopic Guided Superior Hypogastric Plexus Neurolysis in Treating Intractable Pelvic Cancer Pain: A Comparative Study

por Abdelghafar, Ekramy M, Othman, Ahmed H, Soliman, Mahmoud Salem, Kilany, Ayman, Shaaban, Mohammed H, Shaker, Ehab H
Publicado 2021

Kynurenine and oxidative stress in children having learning disorder with and without attention deficit hyperactivity disorder: possible role and involvement

por Kilany, Ayman, Nashaat, Neveen Hassan, Zeidan, Hala M., Hashish, Adel F., El-Saied, Mostafa M., Abdelraouf, Ehab Ragaa
Publicado 2022

Investigating the influence of ubiquinone blood level on the abilities of children with specific learning disorder

por Abdelraouf, Ehab Ragaa, Kilany, Ayman, Hashish, Adel F., Gebril, Ola Hosny, Helal, Suzette Ibrahim, Hasan, Haytham Mohamad, Nashaat, Neveen Hassan
Publicado 2018

BDNF Val66Met Polymorphism: Suggested Genetic Involvement in Some Children with Learning Disorder

por Elhadidy, Mohamed E., Kilany, Ayman, Gebril, Ola Hosny, Nashaat, Neveen Hassan, Zeidan, Hala M., Elsaied, Amal, Hashish, Adel F., Abdelraouf, Ehab Ragaa
Publicado 2022

Dyslexia with and without Irlen syndrome: A study of influence on abilities and brain‐derived neurotrophic factor level

por Abdelraouf, Ehab R., Kilany, Ayman, Elhadidy, Mohamed E., Zeidan, Hala M., Elsaied, Amal, Eid, Ola M., El‐Saied, Mostafa M., Anwar, Rasha, Nashaat, Neveen H.
Publicado 2022