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Minerva Pediatrica
|
October 30, 1978
[A case of Thomsen's disease associated with hypoparathyroidism]
G Cordone, A Iester, V Venzano, et al.
Minerva Pediatrica
|
June 10, 2011
[Epilepsy genetics and genetic epilepsies]
P Striano, A Bianchi, F Zara, et al.
Biochemical and Biophysical Research Communications
|
March 2, 1999
Early decrease of IIx myosin heavy chain transcripts in Duchenne muscular dystrophy
M Pedemonte, C Sandri, S Schiaffino, et al.
Minerva Pediatrica
|
June 15, 1980
[Intracranial hypertension and strabismus in a 5 year old child after nalidixic acid]
L Fasce, R Jamone, G Ragazzini, et al.
International Journal of Oral and Maxillofacial Surgery
|
February 5, 2014
New TASER injuries: lacrimal canaliculus laceration and ethmoid bone fracture
A de Runz, C Minetti, M Brix, et al.
Neuroradiology
|
June 5, 2004
Cerebellar white matter involvement in Salla disease
Roberta Biancheri, A Rossi, M G Mancini, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia
|
July 1, 1983
[A case of annular lipoatrophy (Ferreira-Marques type)]
V Venzano, G Cavallero, C Minetti, et al.
Neurology
|
May 1, 1996
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency
C Minetti, M Bado, G Morreale, et al.
Minerva Pediatrica
|
November 15, 1982
[Clinical and histomorphological study of congenital myopathy with minimal lesions]
G Meola, E Scarpini, C Minetti, et al.
Minerva Pediatrica
|
May 31, 1980
[The association of juvenile diabetes mellitus, primary optic atrophy and deafness (the Wolfram and Ikkos syndrome). Apropos of a personal case]
V Venzano, G Conforti, A Marchesi, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 114) with videos related to
Sort By:
Page
of 12
Minerva Pediatrica
|
October 30, 1978
[A case of Thomsen's disease associated with hypoparathyroidism]
G Cordone, A Iester, V Venzano, et al.
Minerva Pediatrica
|
June 10, 2011
[Epilepsy genetics and genetic epilepsies]
P Striano, A Bianchi, F Zara, et al.
Biochemical and Biophysical Research Communications
|
March 2, 1999
Early decrease of IIx myosin heavy chain transcripts in Duchenne muscular dystrophy
M Pedemonte, C Sandri, S Schiaffino, et al.
Minerva Pediatrica
|
June 15, 1980
[Intracranial hypertension and strabismus in a 5 year old child after nalidixic acid]
L Fasce, R Jamone, G Ragazzini, et al.
International Journal of Oral and Maxillofacial Surgery
|
February 5, 2014
New TASER injuries: lacrimal canaliculus laceration and ethmoid bone fracture
A de Runz, C Minetti, M Brix, et al.
Neuroradiology
|
June 5, 2004
Cerebellar white matter involvement in Salla disease
Roberta Biancheri, A Rossi, M G Mancini, et al.
Giornale Italiano Di Dermatologia E Venereologia : Organo Ufficiale, Societa Italiana Di Dermatologia E Sifilografia
|
July 1, 1983
[A case of annular lipoatrophy (Ferreira-Marques type)]
V Venzano, G Cavallero, C Minetti, et al.
Neurology
|
May 1, 1996
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency
C Minetti, M Bado, G Morreale, et al.
Minerva Pediatrica
|
November 15, 1982
[Clinical and histomorphological study of congenital myopathy with minimal lesions]
G Meola, E Scarpini, C Minetti, et al.
Minerva Pediatrica
|
May 31, 1980
[The association of juvenile diabetes mellitus, primary optic atrophy and deafness (the Wolfram and Ikkos syndrome). Apropos of a personal case]
V Venzano, G Conforti, A Marchesi, et al.
Page
of 12