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Ivan Ivanovski

Showing results (21-30 of 57) with videos related to

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Clinical Dysmorphology|March 2, 2018
Complex cranio-vertebral malformation: disruption sequence or iniencephaly?Marzia Pollazzon, Simonetta Rosato, Ivan Ivanovski, et al.
Irish Journal of Medical Science|May 4, 2020
Predictive value of CRP/albumin ratio in major abdominal surgeryNoel E Donlon, Helen Mohan, Ross Free, et al.
European Journal of Pediatrics|August 27, 2016
Natural history and life-threatening complications in Myhre syndrome and review of the literatureLivia Garavelli, Ilenia Maini, Federica Baccilieri, et al.
Molecular Genetics & Genomic Medicine|February 14, 2023
The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathiesAnna Grether, Ivan Ivanovski, Martina Russo, et al.
Irish Journal of Medical Science|August 16, 2019
Over-admission and over-treatment of patients with cellulitis: a 5-year audit against international guidelinesAilbhe Kiely, Sami Abd Elwahab, Declan McDonnell, et al.
Molecular Syndromology|February 15, 2024
Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant - A Case Report and a Brief Review of the LiteratureMargherita Baga, Ivan Ivanovski, Gianluca Contrò, et al.
Journal of Human Genetics|October 29, 2019
Alazami syndrome: the first case of papillary thyroid carcinomaIvan Ivanovski, Stefano Giuseppe Caraffi, Elisa Magnani, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypesIvan Ivanovski, Susan Akbaroghli, Marzia Pollazzon, et al.
European Journal of Human Genetics : EJHG|April 3, 2023
The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohortPaolo Zanoni, Katharina Steindl, Heinrich Sticht, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11Margherita Lucia De Bernardi, Ivan Ivanovski, Stefano Giuseppe Caraffi, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Clinical Dysmorphology|March 2, 2018
Complex cranio-vertebral malformation: disruption sequence or iniencephaly?Marzia Pollazzon, Simonetta Rosato, Ivan Ivanovski, et al.
Irish Journal of Medical Science|May 4, 2020
Predictive value of CRP/albumin ratio in major abdominal surgeryNoel E Donlon, Helen Mohan, Ross Free, et al.
European Journal of Pediatrics|August 27, 2016
Natural history and life-threatening complications in Myhre syndrome and review of the literatureLivia Garavelli, Ilenia Maini, Federica Baccilieri, et al.
Molecular Genetics & Genomic Medicine|February 14, 2023
The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathiesAnna Grether, Ivan Ivanovski, Martina Russo, et al.
Irish Journal of Medical Science|August 16, 2019
Over-admission and over-treatment of patients with cellulitis: a 5-year audit against international guidelinesAilbhe Kiely, Sami Abd Elwahab, Declan McDonnell, et al.
Molecular Syndromology|February 15, 2024
Novel Insights from Clinical Practice: Xia-Gibbs Syndrome with Pes Cavus, Conjunctival Melanosis, and Eye Asymmetry due to a de novo AHDC1 Gene Variant - A Case Report and a Brief Review of the LiteratureMargherita Baga, Ivan Ivanovski, Gianluca Contrò, et al.
Journal of Human Genetics|October 29, 2019
Alazami syndrome: the first case of papillary thyroid carcinomaIvan Ivanovski, Stefano Giuseppe Caraffi, Elisa Magnani, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypesIvan Ivanovski, Susan Akbaroghli, Marzia Pollazzon, et al.
European Journal of Human Genetics : EJHG|April 3, 2023
The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohortPaolo Zanoni, Katharina Steindl, Heinrich Sticht, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Prominent and elongated coccyx, a new manifestation of KBG syndrome associated with novel mutation in ANKRD11Margherita Lucia De Bernardi, Ivan Ivanovski, Stefano Giuseppe Caraffi, et al.
Pageof 6