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Muhannad Daana

Showing results (1-10 of 18) with videos related to

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Journal of Child Neurology|August 11, 2007
Lamotrigine overdose in a childMuhannad Daana, Yoram Nevo, Ariel Tenenbaum, et al.
Pediatrics|January 5, 2006
Symptomatic myocardial bridging in a child without hypertrophic cardiomyopathyMuhannad Daana, Isaiah Wexler, Eli Milgalter, et al.
Neurogenetics|August 3, 2019
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic featuresBassam Abu-Libdeh, Motee Ashhab, Maher Shahrour, et al.
European Journal of Human Genetics : EJHG|April 13, 2019
Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delayTamar Harel, Ephrat Levy-Lahad, Muhannad Daana, et al.
The Journal of Biological Chemistry|March 3, 2024
A neurodevelopmental disorder associated with a loss-of-function missense mutation in RAB35Adriana Aguila, Somaya Salah, Gopinath Kulasekaran, et al.
International Journal for Equity in Health|August 7, 2015
Varied utilisation of health provision by Arab and Jewish residents in IsraelJo Southern, Hector Roizin, Muhannad Daana, et al.
Vaccine|January 17, 2015
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.
Plos One|July 30, 2013
Variable myopathic presentation in a single family with novel skeletal RYR1 mutationRuben Attali, Sharon Aharoni, Susan Treves, et al.
Vaccine|May 3, 2016
Vaccine escape of piliated Streptococcus pneumoniae strainsGili Regev-Yochay, Hanaa Jaber, Ayob Hamdan, et al.
Journal of Medical Genetics|June 26, 2021
Loss-of-function variants in <i>DNM1</i> cause a specific form of developmental and epileptic encephalopathy only in biallelic stateGökhan Yigit, Ruth Sheffer, Muhannad Daana, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Child Neurology|August 11, 2007
Lamotrigine overdose in a childMuhannad Daana, Yoram Nevo, Ariel Tenenbaum, et al.
Pediatrics|January 5, 2006
Symptomatic myocardial bridging in a child without hypertrophic cardiomyopathyMuhannad Daana, Isaiah Wexler, Eli Milgalter, et al.
Neurogenetics|August 3, 2019
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic featuresBassam Abu-Libdeh, Motee Ashhab, Maher Shahrour, et al.
European Journal of Human Genetics : EJHG|April 13, 2019
Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delayTamar Harel, Ephrat Levy-Lahad, Muhannad Daana, et al.
The Journal of Biological Chemistry|March 3, 2024
A neurodevelopmental disorder associated with a loss-of-function missense mutation in RAB35Adriana Aguila, Somaya Salah, Gopinath Kulasekaran, et al.
International Journal for Equity in Health|August 7, 2015
Varied utilisation of health provision by Arab and Jewish residents in IsraelJo Southern, Hector Roizin, Muhannad Daana, et al.
Vaccine|January 17, 2015
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.
Plos One|July 30, 2013
Variable myopathic presentation in a single family with novel skeletal RYR1 mutationRuben Attali, Sharon Aharoni, Susan Treves, et al.
Vaccine|May 3, 2016
Vaccine escape of piliated Streptococcus pneumoniae strainsGili Regev-Yochay, Hanaa Jaber, Ayob Hamdan, et al.
Journal of Medical Genetics|June 26, 2021
Loss-of-function variants in <i>DNM1</i> cause a specific form of developmental and epileptic encephalopathy only in biallelic stateGökhan Yigit, Ruth Sheffer, Muhannad Daana, et al.
Pageof 2