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Julia Vodopiutz

Showing results (1-10 of 36) with videos related to

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Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|February 7, 2020
Jannina Sigl, Julia Vodopiutz, Adrian Tanew, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|December 27, 2019
An unusual presentation of incontinentia pigmentiJannina Sigl, Julia Vodopiutz, Adrian Tanew, et al.
Clinical Genetics|March 9, 2026
Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial DysplasiaDorothea Stojanovic, Dorota Garczarczyk-Asim, Julia Vodopiutz, et al.
Journal of Women'S Health (2002)|February 7, 2003
Chest pain in hospitalized patients: cause-specific and gender-specific differencesJulia Vodopiutz, Sabine Poller, Barbara Schneider, et al.
Fetal Diagnosis and Therapy|November 27, 2009
Prenatal diagnosis of apert syndrome with cloverleaf skull deformity using ultrasound, fetal magnetic resonance imaging and genetic analysisBenedikt Weber, Anton H Schwabegger, Julia Vodopiutz, et al.
The British Journal of Ophthalmology|November 13, 2012
Coexistence of KCNV2 associated cone dystrophy with supernormal rod electroretinogram and MFRP related oculopathy in a Turkish familyMarkus Ritter, Julia Vodopiutz, Silvia Lechner, et al.
Wiener Medizinische Wochenschrift (1946)|March 10, 2021
Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and managementNina-Katharina Walleczek, Kristina Förster, Martina Seyr, et al.
Molecular Genetics and Metabolism|June 15, 2007
Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia IIIChike Bellarmine Item, Ivana Mihalek, Oliver Lichtarge, et al.
Genes|November 27, 2021
Expanding the Phenotype of the <i>FAM149B1</i>-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single FamilySandy Siegert, Gabriel T Mindler, Christof Brücke, et al.
Epilepsia|August 28, 2021
The relation of etiology based on the 2017 ILAE classification to the effectiveness of the ketogenic diet in drug-resistant epilepsy in childhoodMarkus Breu, Chiara Häfele, Petra Trimmel-Schwahofer, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|February 7, 2020
Jannina Sigl, Julia Vodopiutz, Adrian Tanew, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|December 27, 2019
An unusual presentation of incontinentia pigmentiJannina Sigl, Julia Vodopiutz, Adrian Tanew, et al.
Clinical Genetics|March 9, 2026
Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial DysplasiaDorothea Stojanovic, Dorota Garczarczyk-Asim, Julia Vodopiutz, et al.
Journal of Women'S Health (2002)|February 7, 2003
Chest pain in hospitalized patients: cause-specific and gender-specific differencesJulia Vodopiutz, Sabine Poller, Barbara Schneider, et al.
Fetal Diagnosis and Therapy|November 27, 2009
Prenatal diagnosis of apert syndrome with cloverleaf skull deformity using ultrasound, fetal magnetic resonance imaging and genetic analysisBenedikt Weber, Anton H Schwabegger, Julia Vodopiutz, et al.
The British Journal of Ophthalmology|November 13, 2012
Coexistence of KCNV2 associated cone dystrophy with supernormal rod electroretinogram and MFRP related oculopathy in a Turkish familyMarkus Ritter, Julia Vodopiutz, Silvia Lechner, et al.
Wiener Medizinische Wochenschrift (1946)|March 10, 2021
Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and managementNina-Katharina Walleczek, Kristina Förster, Martina Seyr, et al.
Molecular Genetics and Metabolism|June 15, 2007
Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia IIIChike Bellarmine Item, Ivana Mihalek, Oliver Lichtarge, et al.
Genes|November 27, 2021
Expanding the Phenotype of the <i>FAM149B1</i>-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single FamilySandy Siegert, Gabriel T Mindler, Christof Brücke, et al.
Epilepsia|August 28, 2021
The relation of etiology based on the 2017 ILAE classification to the effectiveness of the ketogenic diet in drug-resistant epilepsy in childhoodMarkus Breu, Chiara Häfele, Petra Trimmel-Schwahofer, et al.
Pageof 4