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Results of search for 'au:"Banin, P"'
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Authors
Aiello, V
Aloi, C
Andreoli, M
Banin, P
Bergamini, M
Bernardi, F
Bezzi, T M
Calzolari, E
Camerini, G
Cioni, P
D'Annunzio, G
De Ritis, L
De Sanctis, V
Giovannini, M
Malaguti, L
Marchetti, G
Palazzi, P
Patracchini, P
Pecorari, R
Trombini, R
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Topics
Adolescent
Age Factors
Autoimmunity
Calcinosis
Celiac Disease
Child
Child, Preschool
Chondroblastoma
Chromosome Banding
Chromosome Mapping
Chromosomes, Human, Pair 22
Coma
DNA
Ectodermal Dysplasia
Female
Humans
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Syndrome
etiology
genetics
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English
Italian
Your search returned 7 results.
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1.
[Persistent left gonalgia in an adolescent affected by left femoral chondroblastoma].
[electronic resource]
by
Banin, P
Malaguti, L
De Sanctis, V
Producer:
20020206
In:
Minerva pediatrica
vol. 53
Availability:
No items available.
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2.
[Hypertension, convulsive crises and coma in patients with thalassemia major following multiple blood transfusions].
[electronic resource]
by
Bezzi, T M
Trombini, R
Bergamini, M
Banin, P
Producer:
19821202
In:
Minerva pediatrica
vol. 34
Availability:
No items available.
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3.
Regression of autoimmunity and abnormal glucose homeostasis in an adolescent boy with silent coeliac disease.
[electronic resource]
by
Banin, P
Perretta, R
Ravaioli, E
De Sanctis, V
Producer:
20030221
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 91
Online resources:
Available from publisher's website
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4.
[Anhidrotic ectodermal dysplasia in females].
[electronic resource]
by
Bezzi, T M
Banin, P
Virgilli, A R
Trombini, R
Camerini, G
Producer:
19821218
In:
Minerva pediatrica
vol. 34
Availability:
No items available.
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5.
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.
[electronic resource]
by
Patracchini, P
Calzolari, E
Aiello, V
Palazzi, P
Banin, P
Marchetti, G
Bernardi, F
Producer:
19891116
In:
Human genetics
vol. 83
Online resources:
Available from publisher's website
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No items available.
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6.
[Goltz syndrome].
[electronic resource]
by
Pecorari, R
Banin, P
De Ritis, L
Cioni, P
Andreoli, M
Ultori, E
Solaroli, C
Sgarbanti, E
Producer:
19870109
In:
La Pediatria medica e chirurgica : Medical and surgical pediatrics
vol. 8
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7.
A novel hepatocyte nuclear factor-1β (MODY 5) gene mutation in a Romanian boy with pancreatic calcifications, renal and hepatic dysfunction.
[electronic resource]
by
Banin, P
Giovannini, M
Raimondi, F
D'Annunzio, G
Sala, S
Salina, A
Aloi, C
De Sanctis, V
Producer:
20110916
In:
Georgian medical news
no. 193
Availability:
No items available.
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