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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 disease
P 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) translocation
P 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 dysfunction
P Banin, M Giovannini, F Raimondi, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 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 disease
P 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) translocation
P 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 dysfunction
P Banin, M Giovannini, F Raimondi, et al.
Page
of 1