Search research articles
Contact Us
Filters
Showing results (291-300 of 566) with videos related to
Page
of 57
Sort By:
Frontiers in Endocrinology
|
October 1, 2024
Recurrent laryngeal nerve monitoring by flexible laryngoscopy during thyroid radiofrequency ablation in the awake patient
Marsida Teliti, Antonio Occhini, Rodolfo Fonte, et al.
Journal of Clinical Medicine
|
May 25, 2024
Does Thoracic Duct Ligation at the Time of Esophagectomy Impact Long-Term Survival? An Individual Patient Data Meta-Analysis
Alberto Aiolfi, Davide Bona, Matteo Calì, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
December 3, 2020
Possible implication of undescribed SMN1-SMN2 genotype in chronic EMG-pattern of SMA with transitory acute denervation
Girolamo A Vitello, Francesco Calì, Mirella Vinci, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
May 11, 2020
Evaluation of perioperative complications using a newly described staging system for placenta accreta spectrum
Andrea Dall'Asta, Giuseppe Calì, Francesco Forlani, et al.
American Journal of Medical Genetics
|
May 26, 1999
FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes
D Giardino, D Bettio, G Gottardi, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Intracranial gene delivery of LV-NAGLU vector corrects neuropathology in murine MPS IIIB
Carmela Di Domenico, Guglielmo R D Villani, Daniele Di Napoli, et al.
Clinical Genetics
|
January 26, 2007
1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features
A Alberti, C Romano, M Falco, et al.
Scientific Reports
|
March 13, 2019
Publisher Correction: Parkin-dependent regulation of the MCU complex component MICU1
Alessandra Matteucci, Maria Patron, Denis Vecellio Reane, et al.
Scientific Reports
|
July 9, 2024
A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disability
Mirella Vinci, Simone Treccarichi, Rosanna Galati Rando, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 21, 2011
Clinical correlates of quality of life in Tourette syndrome
Clare M Eddy, Andrea E Cavanna, Mariangela Gulisano, et al.
Page
of 57
Search research articles
Search
Showing results (291-300 of 566) with videos related to
Sort By:
Page
of 57
Frontiers in Endocrinology
|
October 1, 2024
Recurrent laryngeal nerve monitoring by flexible laryngoscopy during thyroid radiofrequency ablation in the awake patient
Marsida Teliti, Antonio Occhini, Rodolfo Fonte, et al.
Journal of Clinical Medicine
|
May 25, 2024
Does Thoracic Duct Ligation at the Time of Esophagectomy Impact Long-Term Survival? An Individual Patient Data Meta-Analysis
Alberto Aiolfi, Davide Bona, Matteo Calì, et al.
Journal of Musculoskeletal & Neuronal Interactions
|
December 3, 2020
Possible implication of undescribed SMN1-SMN2 genotype in chronic EMG-pattern of SMA with transitory acute denervation
Girolamo A Vitello, Francesco Calì, Mirella Vinci, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
May 11, 2020
Evaluation of perioperative complications using a newly described staging system for placenta accreta spectrum
Andrea Dall'Asta, Giuseppe Calì, Francesco Forlani, et al.
American Journal of Medical Genetics
|
May 26, 1999
FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes
D Giardino, D Bettio, G Gottardi, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Intracranial gene delivery of LV-NAGLU vector corrects neuropathology in murine MPS IIIB
Carmela Di Domenico, Guglielmo R D Villani, Daniele Di Napoli, et al.
Clinical Genetics
|
January 26, 2007
1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features
A Alberti, C Romano, M Falco, et al.
Scientific Reports
|
March 13, 2019
Publisher Correction: Parkin-dependent regulation of the MCU complex component MICU1
Alessandra Matteucci, Maria Patron, Denis Vecellio Reane, et al.
Scientific Reports
|
July 9, 2024
A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disability
Mirella Vinci, Simone Treccarichi, Rosanna Galati Rando, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 21, 2011
Clinical correlates of quality of life in Tourette syndrome
Clare M Eddy, Andrea E Cavanna, Mariangela Gulisano, et al.
Page
of 57