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World Neurosurgery
|
November 19, 2018
Intraspinal Inclusion Tumor After Myelomeningocele Repair: A Long-Term Single-Center Experience
Pietro Fiaschi, Gianluca Piatelli, Armando Cama, et al.
Journal of Genetics
|
June 18, 2019
'Distal 16p12.2 microdeletion' in a patient with autosomal recessive deafness-22
Elisa Tassano, Patrizia Ronchetto, Annalisa Calcagno, et al.
Journal of Pediatric Hematology/Oncology
|
May 25, 2010
Simultaneous occurrence of pancreatoblastoma and neuroblastoma in a newborn with beckwith-wiedemann syndrome
Stefania Sorrentino, Massimo Conte, Paolo Nozza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 7, 2021
A rare triad of morning glory disc anomaly, moyamoya vasculopathy, and transsphenoidal cephalocele: pathophysiological considerations and surgical management
Marco Pavanello, Pietro Fiaschi, Andrea Accogli, et al.
Prenatal Diagnosis
|
May 20, 2024
Truncating variants in PAPSS2 gene: A cause of early prenatal onset brachyolmia?
Giulia Biancotto, Giulia Rosti, Francesca Madia, et al.
Journal of Clinical Laboratory Analysis
|
November 17, 2011
Troubleshooting fine-tuning procedures for qPCR system design
Alessandro Raso, Samantha Mascelli, Paolo Nozza, et al.
European Journal of Medical Genetics
|
December 15, 2015
Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits
Elisa Tassano, Andrea Accogli, Marco Pavanello, et al.
BMC Medical Genetics
|
October 6, 2012
Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAE genes in a family with developmental delay and behavioural problems
Valeria Capra, Marisol Mirabelli-Badenier, Michela Stagnaro, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
July 10, 2013
Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defects
Elisa Merello, Zoha Kibar, Redouane Allache, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
August 7, 2019
Chiari malformation type I: what information from the genetics?
Valeria Capra, Michele Iacomino, Andrea Accogli, et al.
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Search research articles
Search
Showing results (11-20 of 176) with videos related to
Sort By:
Page
of 18
World Neurosurgery
|
November 19, 2018
Intraspinal Inclusion Tumor After Myelomeningocele Repair: A Long-Term Single-Center Experience
Pietro Fiaschi, Gianluca Piatelli, Armando Cama, et al.
Journal of Genetics
|
June 18, 2019
'Distal 16p12.2 microdeletion' in a patient with autosomal recessive deafness-22
Elisa Tassano, Patrizia Ronchetto, Annalisa Calcagno, et al.
Journal of Pediatric Hematology/Oncology
|
May 25, 2010
Simultaneous occurrence of pancreatoblastoma and neuroblastoma in a newborn with beckwith-wiedemann syndrome
Stefania Sorrentino, Massimo Conte, Paolo Nozza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 7, 2021
A rare triad of morning glory disc anomaly, moyamoya vasculopathy, and transsphenoidal cephalocele: pathophysiological considerations and surgical management
Marco Pavanello, Pietro Fiaschi, Andrea Accogli, et al.
Prenatal Diagnosis
|
May 20, 2024
Truncating variants in PAPSS2 gene: A cause of early prenatal onset brachyolmia?
Giulia Biancotto, Giulia Rosti, Francesca Madia, et al.
Journal of Clinical Laboratory Analysis
|
November 17, 2011
Troubleshooting fine-tuning procedures for qPCR system design
Alessandro Raso, Samantha Mascelli, Paolo Nozza, et al.
European Journal of Medical Genetics
|
December 15, 2015
Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits
Elisa Tassano, Andrea Accogli, Marco Pavanello, et al.
BMC Medical Genetics
|
October 6, 2012
Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAE genes in a family with developmental delay and behavioural problems
Valeria Capra, Marisol Mirabelli-Badenier, Michela Stagnaro, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
July 10, 2013
Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defects
Elisa Merello, Zoha Kibar, Redouane Allache, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
August 7, 2019
Chiari malformation type I: what information from the genetics?
Valeria Capra, Michele Iacomino, Andrea Accogli, et al.
Page
of 18