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Shazia Maqbool

Showing results (11-20 of 35) with videos related to

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BJGP Open|December 20, 2018
Is integrated private-clinic based early child development care effective? A clustered randomised trial in PakistanMuhammad Amir Khan, Syeda Somyyah Owais, Shazia Maqbool, et al.
Children (Basel, Switzerland)|June 28, 2023
Supporting Depressed Mothers of Young Children with Intellectual Disability: Feasibility of an Integrated Parenting Intervention in a Low-Income SettingNasim Chaudhry, Rabia Sattar, Tayyeba Kiran, et al.
European Journal of Medical Genetics|September 19, 2022
AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic rangeKamran Salayev, Clarissa Rocca, Rauan Kaiyrzhanov, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphismFatima Rahman, Luisa Marsili, Domizia Pasquetti, et al.
Journal of Medical Genetics|December 29, 2022
Consolidating the association of biallelic <i>MAPKAPK5</i> pathogenic variants with a distinct syndromic neurodevelopmental disorderReza Maroofian, Stephanie Efthymiou, Mohnish Suri, et al.
Journal of Health, Population, and Nutrition|December 13, 2023
Establishing performance standards for child development: learnings from the ECDI2030Nicole Petrowski, Filipa de Castro, Susan Davis-Becker, et al.
European Journal of Human Genetics : EJHG|June 24, 2021
Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric featuresMaha S Zaki, Andrea Accogli, Ghayda Mirzaa, et al.
Clinical Genetics|February 15, 2024
Expanding the phenotype of PPP1R21-related neurodevelopmental disorderMohammed Almannai, Dana Marafi, Maha S Zaki, et al.
Ebiomedicine|May 10, 2025
SLK is mutated in individuals with a neurodevelopmental disorderLama Alabdi, Norah Altuwaijri, Jun-Yi Zhu, et al.
Journal of Medical Genetics|November 11, 2020
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndromePasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
BJGP Open|December 20, 2018
Is integrated private-clinic based early child development care effective? A clustered randomised trial in PakistanMuhammad Amir Khan, Syeda Somyyah Owais, Shazia Maqbool, et al.
Children (Basel, Switzerland)|June 28, 2023
Supporting Depressed Mothers of Young Children with Intellectual Disability: Feasibility of an Integrated Parenting Intervention in a Low-Income SettingNasim Chaudhry, Rabia Sattar, Tayyeba Kiran, et al.
European Journal of Medical Genetics|September 19, 2022
AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic rangeKamran Salayev, Clarissa Rocca, Rauan Kaiyrzhanov, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphismFatima Rahman, Luisa Marsili, Domizia Pasquetti, et al.
Journal of Medical Genetics|December 29, 2022
Consolidating the association of biallelic <i>MAPKAPK5</i> pathogenic variants with a distinct syndromic neurodevelopmental disorderReza Maroofian, Stephanie Efthymiou, Mohnish Suri, et al.
Journal of Health, Population, and Nutrition|December 13, 2023
Establishing performance standards for child development: learnings from the ECDI2030Nicole Petrowski, Filipa de Castro, Susan Davis-Becker, et al.
European Journal of Human Genetics : EJHG|June 24, 2021
Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric featuresMaha S Zaki, Andrea Accogli, Ghayda Mirzaa, et al.
Clinical Genetics|February 15, 2024
Expanding the phenotype of PPP1R21-related neurodevelopmental disorderMohammed Almannai, Dana Marafi, Maha S Zaki, et al.
Ebiomedicine|May 10, 2025
SLK is mutated in individuals with a neurodevelopmental disorderLama Alabdi, Norah Altuwaijri, Jun-Yi Zhu, et al.
Journal of Medical Genetics|November 11, 2020
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndromePasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, et al.
Pageof 4