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P Banin

Showing results (1-10 of 7) with videos related to

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Minerva Pediatrica|October 23, 2001
[Persistent left gonalgia in an adolescent affected by left femoral chondroblastoma]P Banin, L Malaguti, V De Sanctis
Acta Paediatrica (Oslo, Norway : 1992)|November 19, 2002
Regression of autoimmunity and abnormal glucose homeostasis in an adolescent boy with silent coeliac diseaseP Banin, R Perretta, E Ravaioli, et al.
Minerva Pediatrica|May 15, 1982
[Hypertension, convulsive crises and coma in patients with thalassemia major following multiple blood transfusions]T M Bezzi, R Trombini, M Bergamini, et al.
Minerva Pediatrica|June 15, 1982
[Anhidrotic ectodermal dysplasia in females]T M Bezzi, P Banin, A R Virgilli, et al.
Human Genetics|October 1, 1989
Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocationP Patracchini, E Calzolari, V Aiello, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1986
[Goltz syndrome]R Pecorari, P Banin, L De Ritis, et al.
Georgian Medical News|May 28, 2011
A novel hepatocyte nuclear factor-1β (MODY 5) gene mutation in a Romanian boy with pancreatic calcifications, renal and hepatic dysfunctionP Banin, M Giovannini, F Raimondi, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Minerva Pediatrica|October 23, 2001
[Persistent left gonalgia in an adolescent affected by left femoral chondroblastoma]P Banin, L Malaguti, V De Sanctis
Acta Paediatrica (Oslo, Norway : 1992)|November 19, 2002
Regression of autoimmunity and abnormal glucose homeostasis in an adolescent boy with silent coeliac diseaseP Banin, R Perretta, E Ravaioli, et al.
Minerva Pediatrica|May 15, 1982
[Hypertension, convulsive crises and coma in patients with thalassemia major following multiple blood transfusions]T M Bezzi, R Trombini, M Bergamini, et al.
Minerva Pediatrica|June 15, 1982
[Anhidrotic ectodermal dysplasia in females]T M Bezzi, P Banin, A R Virgilli, et al.
Human Genetics|October 1, 1989
Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocationP Patracchini, E Calzolari, V Aiello, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1986
[Goltz syndrome]R Pecorari, P Banin, L De Ritis, et al.
Georgian Medical News|May 28, 2011
A novel hepatocyte nuclear factor-1β (MODY 5) gene mutation in a Romanian boy with pancreatic calcifications, renal and hepatic dysfunctionP Banin, M Giovannini, F Raimondi, et al.
Pageof 1