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Jacek Majewski

Showing results (121-130 of 333) with videos related to

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Arthritis Research & Therapy|August 15, 2013
Identification of three new cis-regulatory IRF5 polymorphisms: in vitro studiesElisa Alonso-Perez, Romina Fernandez-Poceiro, Emilie Lalonde, et al.
Human Molecular Genetics|September 13, 2014
A polyadenylation site variant causes transcript-specific BMP1 deficiency and frequent fractures in childrenSomayyeh Fahiminiya, Hadil Al-Jallad, Jacek Majewski, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 12, 2014
Osteoporosis caused by mutations in PLS3: clinical and bone tissue characteristicsSomayyeh Fahiminiya, Jacek Majewski, Hadil Al-Jallad, et al.
Sensors (Basel, Switzerland)|February 26, 2025
Thermoelectric Measuring Equipment for Perioperative Monitoring of Temperature and Heat Flux Density of the Human Eye in Vitreoretinal SurgeryRoman Kobylianskyi, Krzysztof Przystupa, Valentyn Lysko, et al.
Clinical Genetics|February 5, 2025
Two Novel Protein-Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal ComplexZeynep Yalcin, Zheng Gao, Ibrahim M Abdelrazek, et al.
Kardiologia Polska|March 21, 2012
Effect of selected prothrombotic and proinflammatory factors on the incidence of venous thrombosis after pacemaker implantationJacek Lelakowski, Teresa Barbara Domagała, Anna Rydlewska, et al.
American Journal of Medical Genetics. Part A|April 23, 2017
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feetMelanie Lacaria, Myriam Srour, Jacques L Michaud, et al.
American Journal of Medical Genetics. Part A|June 19, 2014
Contribution of RIT1 mutations to the pathogenesis of Noonan syndrome: four new cases and further evidence of heterogeneityMonika Gos, Somayyeh Fahiminiya, Jarosław Poznański, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 14, 2003
Lack of an association of apolipoprotein E gene polymorphisms with familial age-related macular degenerationDennis W Schultz, Michael L Klein, Andrea Humpert, et al.
Neurogenetics|February 27, 2016
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxiaYi-Hong Shao, Karine Choquet, Roberta La Piana, et al.
Pageof 34

Showing results (121-130 of 333) with videos related to

Sort By:
Pageof 34
Arthritis Research & Therapy|August 15, 2013
Identification of three new cis-regulatory IRF5 polymorphisms: in vitro studiesElisa Alonso-Perez, Romina Fernandez-Poceiro, Emilie Lalonde, et al.
Human Molecular Genetics|September 13, 2014
A polyadenylation site variant causes transcript-specific BMP1 deficiency and frequent fractures in childrenSomayyeh Fahiminiya, Hadil Al-Jallad, Jacek Majewski, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 12, 2014
Osteoporosis caused by mutations in PLS3: clinical and bone tissue characteristicsSomayyeh Fahiminiya, Jacek Majewski, Hadil Al-Jallad, et al.
Sensors (Basel, Switzerland)|February 26, 2025
Thermoelectric Measuring Equipment for Perioperative Monitoring of Temperature and Heat Flux Density of the Human Eye in Vitreoretinal SurgeryRoman Kobylianskyi, Krzysztof Przystupa, Valentyn Lysko, et al.
Clinical Genetics|February 5, 2025
Two Novel Protein-Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal ComplexZeynep Yalcin, Zheng Gao, Ibrahim M Abdelrazek, et al.
Kardiologia Polska|March 21, 2012
Effect of selected prothrombotic and proinflammatory factors on the incidence of venous thrombosis after pacemaker implantationJacek Lelakowski, Teresa Barbara Domagała, Anna Rydlewska, et al.
American Journal of Medical Genetics. Part A|April 23, 2017
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feetMelanie Lacaria, Myriam Srour, Jacques L Michaud, et al.
American Journal of Medical Genetics. Part A|June 19, 2014
Contribution of RIT1 mutations to the pathogenesis of Noonan syndrome: four new cases and further evidence of heterogeneityMonika Gos, Somayyeh Fahiminiya, Jarosław Poznański, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 14, 2003
Lack of an association of apolipoprotein E gene polymorphisms with familial age-related macular degenerationDennis W Schultz, Michael L Klein, Andrea Humpert, et al.
Neurogenetics|February 27, 2016
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxiaYi-Hong Shao, Karine Choquet, Roberta La Piana, et al.
Pageof 34