نتائج البحث - "Mensuda Hasanhodzic"

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دورية أكاديمية

Neonatal bacterial meningitis: Results from a cross-sectional hospital based study

المؤلفون: Izeta Softić, Husref Tahirović, Mensuda Hasanhodžić

المصدر: Acta Medica Academica, Vol 44, Iss 2, Pp 117-123 (2015)

مصطلحات موضوعية: Meningitis, Newborn, Neonatal intensive care unit, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://ama.ba/index.php/ama/article/view/252/pdf; https://doaj.org/toc/1840-1848; https://doaj.org/toc/1840-2879

URL الوصول: https://doaj.org/article/86ece04b2b004a0383fe07f373acc0b4

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دورية أكاديمية

Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.

المؤلفون: Tina Likar, Mensuda Hasanhodžić, Nataša Teran, Aleš Maver, Borut Peterlin, Karin Writzl

المصدر: PLoS ONE, Vol 13, Iss 1, p e0188578 (2018)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5749682?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/74d4157805a4410f8f4613f8187ecc8e

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دورية أكاديمية

Down Syndrome and Thyroid Gland

المؤلفون: Mensuda Hasanhodžić, Husref Tahirović, Ljerka Lukinac

المصدر: Biomolecules & Biomedicine, Vol 6, Iss 3 (2006)

مصطلحات موضوعية: down syndrome, thyroid gland, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.bjbms.org/ojs/index.php/bjbms/article/view/3142; https://doaj.org/toc/2831-0896; https://doaj.org/toc/2831-090X

URL الوصول: https://doaj.org/article/696b7c47379246ad9a0361d57dac2a45

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دورية أكاديمية

FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

المؤلفون: Elyssa Cannaerts, Anju Shukla, Mensuda Hasanhodzic, Maaike Alaerts, Dorien Schepers, Lut Van Laer, Katta M. Girisha, Iva Hojsak, Bart Loeys, Aline Verstraeten

المصدر: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-13 (2018)

مصطلحات موضوعية: Periventricular nodular heterotopia, Live-born males, Filaminopathy, Connective tissue disease, Internal medicine, RC31-1245, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12881-018-0655-0; https://doaj.org/toc/1471-2350

URL الوصول: https://doaj.org/article/d0f83f1afa7b4a4bb15e3385ed6429ce

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FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

المؤلفون: Lut Van Laer, Iva Hojsak, Maaike Alaerts, Dorien Schepers, Anju Shukla, Aline Verstraeten, Mensuda Hasanhodzic, Elyssa Cannaerts, Katta M. Girisha, Bart Loeys

المصدر: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-13 (2018)
BMC Medical Genetics
BMC medical genetics

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, Case Report, 030105 genetics & heredity, 0302 clinical medicine, Genes, X-Linked, Medicine, Mitral valve prolapse, FLNA, Missense mutation, Live-born males, Child, Connective Tissue Diseases, Genetics (clinical), Middle Aged, Connective tissue disease, 3. Good health, Pedigree, Periventricular nodular heterotopia, medicine.anatomical_structure, Phenotype, Connective Tissue, Child, Preschool, Joint hypermobility, Adult, medicine.medical_specialty, lcsh:Internal medicine, Adolescent, Genotype, lcsh:QH426-470, Filamins, Connective tissue, 03 medical and health sciences, Young Adult, Pectus excavatum, Genetics, Humans, Filaminopathy, lcsh:RC31-1245, business.industry, Infant, Newborn, medicine.disease, Pulmonary hypertension, lcsh:Genetics, Mutation, Ehlers-Danlos Syndrome, Human medicine, business, 030217 neurology & neurosurgery

وصف الملف: pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d91e8a5fd439505a6f7cf9c9217af189
http://link.springer.com/article/10.1186/s12881-018-0655-0

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Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a developing country

المؤلفون: Meliha Stomornjak-Vukadin, Senka Mesihović-Dinarević, Lejla Mehinovic, Ilvana Kurtovic-Basic, Mensuda Hasanhodzic, Feriha Catibusic, Amina Kurtovic-Kozaric, Mirza Kozaric, Darinka Šumanović Glamuzina

المصدر: Bosnian Journal of Basic Medical Sciences
Bosnian Journal of Basic Medical Sciences, Vol 16, Iss 2 (2016)

مصطلحات موضوعية: Williams Syndrome, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Pediatrics, medicine.medical_specialty, Short Report, Microdeletion syndrome, 030105 genetics & heredity, Single Center, 03 medical and health sciences, DiGeorge syndrome, DiGeorge Syndrome, medicine, Humans, Child, Developing Countries, In Situ Hybridization, Fluorescence, Bosnia and Herzegovina, lcsh:R5-920, medicine.diagnostic_test, business.industry, Incidence, Incidence (epidemiology), Genetic Diseases, Inborn, Wolf-Hirschhorn, nutritional and metabolic diseases, Syndrome, General Medicine, Gene deletion, medicine.disease, Williams, nervous system diseases, Angelman, fluorescent in situ hybridization, DiGeorge, Fish , Prader-Willi, Williams syndrome, Chromosome Deletion, lcsh:Medicine (General), business, Gene Deletion, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89be54cf45b68ffee653b22a5279fbda
https://doi.org/10.17305/bjbms.2016.994

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Down Syndrome and Thyroid Gland

المؤلفون: Husref Tahirović, Ljerka Lukinac, Mensuda Hasanhodzic

المصدر: Bosnian Journal of Basic Medical Sciences, Vol 6, Iss 3 (2006)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6a4ada6ec3de5e3599c7c961e660149
http://www.bjbms.org/ojs/index.php/bjbms/article/view/3142

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Additional file 1: of FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

المؤلفون: Cannaerts, Elyssa, Shukla, Anju, Mensuda Hasanhodzic, Alaerts, Maaike, Schepers, Dorien, Lut Van Laer, Katta Girisha, Hojsak, Iva, Loeys, Bart, Verstraeten, Aline

مصطلحات موضوعية: 3. Good health

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::57a6f62ea7b3eea2be20ed00e8f2ac33

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Additional file 2: of FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

المؤلفون: Cannaerts, Elyssa, Shukla, Anju, Mensuda Hasanhodzic, Alaerts, Maaike, Schepers, Dorien, Lut Van Laer, Katta Girisha, Hojsak, Iva, Loeys, Bart, Verstraeten, Aline

مصطلحات موضوعية: 3. Good health

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::09524797f3a16eef90802a20c7c160c4

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Additional file 1: of FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

المؤلفون: Cannaerts, Elyssa, Shukla, Anju, Mensuda Hasanhodzic, Alaerts, Maaike, Schepers, Dorien, Lut Van Laer, Katta Girisha, Hojsak, Iva, Loeys, Bart, Verstraeten, Aline

مصطلحات موضوعية: 3. Good health

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::29159b89342291dd1a045857edf1f506

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