Muhannad Daana

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Sharon Aharoni, Menachem Sadeh, Yehuda Shapira et al. · Neuromuscular Disorders · 2016 · 36 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Biallelic variants in AGTPBP1, involved in tubulin deglutamylation, are associated with cerebellar degeneration and motor neuropathy

Ruth Sheffer, Michal Gur, Rebecca Brooks et al. · European Journal of Human Genetics · 2019 · 35 citations · Full text

Life Sciences, Genetics, Neuroscience +15

Measuring the effects of pneumococcal conjugate vaccine (PCV7) on Streptococcus pneumoniae carriage and antibiotic resistance: The Palestinian-Israeli Collaborative Research (PICR)

Muhannad Daana, Galia Rahav, Ayob Hamdan et al. · Vaccine · 2015 · 29 citations

Veterinary Medicine, Infectious Diseases, Microbiology +17

Infantile SOD1 deficiency syndrome caused by a homozygous <i>SOD1</i> variant with absence of enzyme activity

Shlomit Ezer, Muhannad Daana, Julien H. Park et al. · Brain · 2021 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway

Simon Edvardson, Guoling Tian, Hayley Cullen et al. · Human Molecular Genetics · 2016 · 25 citations · Full text

Life Sciences, Molecular Genetics, Neurology +17