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Minerva Pediatrica
|
September 24, 2013
[What new fathers know, think and do: a survey about fathering's attitudes, beliefs and behaviors in a sample of 570 men just after the birth of their newborn]
A Pellai, F Festa, F Cilento, et al.
Royal Society Open Science
|
April 8, 2020
Fluid-structure interaction simulations outperform computational fluid dynamics in the description of thoracic aorta haemodynamics and in the differentiation of progressive dilation in Marfan syndrome patients
R Pons, A Guala, J F Rodríguez-Palomares, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1997
[Malformations of the midline. A case-control study]
A Guala, G Pastore, P Cerruti Mainardi, et al.
Minerva Pediatrica
|
July 14, 2004
[Prevalence of breast feeding at the ASL 11--Piedmont Region]
A Guala, M Cozzi, D Campra, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 25, 2011
[Prevalence of breastfeeding in the Verbano-Cusio-Ossola region]
A Guala, L Boscardini, L Azioni, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
October 15, 2019
Decreased rotational flow and circumferential wall shear stress as early markers of descending aorta dilation in Marfan syndrome: a 4D flow CMR study
A Guala, G Teixido-Tura, L Dux-Santoy, et al.
Minerva Pediatrica
|
October 1, 1996
The Williams syndrome: an Italian collaborative study
P Franceschini, A Guala, M P Vardeu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 18, 2020
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations
R Villa, V G C Fergnani, R Silipigni, et al.
Journal of Medical Genetics
|
November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
E H Stover, K J Borthwick, C Bavalia, et al.
Clinical Genetics
|
March 16, 2017
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes
E Di Gregorio, E Riberi, E F Belligni, et al.
Page
of 10
Search research articles
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Showing results (91-100 of 100) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 100 results.
Minerva Pediatrica
|
September 24, 2013
[What new fathers know, think and do: a survey about fathering's attitudes, beliefs and behaviors in a sample of 570 men just after the birth of their newborn]
A Pellai, F Festa, F Cilento, et al.
Royal Society Open Science
|
April 8, 2020
Fluid-structure interaction simulations outperform computational fluid dynamics in the description of thoracic aorta haemodynamics and in the differentiation of progressive dilation in Marfan syndrome patients
R Pons, A Guala, J F Rodríguez-Palomares, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1997
[Malformations of the midline. A case-control study]
A Guala, G Pastore, P Cerruti Mainardi, et al.
Minerva Pediatrica
|
July 14, 2004
[Prevalence of breast feeding at the ASL 11--Piedmont Region]
A Guala, M Cozzi, D Campra, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 25, 2011
[Prevalence of breastfeeding in the Verbano-Cusio-Ossola region]
A Guala, L Boscardini, L Azioni, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
October 15, 2019
Decreased rotational flow and circumferential wall shear stress as early markers of descending aorta dilation in Marfan syndrome: a 4D flow CMR study
A Guala, G Teixido-Tura, L Dux-Santoy, et al.
Minerva Pediatrica
|
October 1, 1996
The Williams syndrome: an Italian collaborative study
P Franceschini, A Guala, M P Vardeu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 18, 2020
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations
R Villa, V G C Fergnani, R Silipigni, et al.
Journal of Medical Genetics
|
November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
E H Stover, K J Borthwick, C Bavalia, et al.
Clinical Genetics
|
March 16, 2017
Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes
E Di Gregorio, E Riberi, E F Belligni, et al.
Page
of 10