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Minerva Pediatrica
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May 1, 1997
[Ehlers-Danlos syndrome type I. Ultrastructural study]
M Paradisi, L Giubilei, F Canzona, et al.
Vascular
|
April 7, 2009
Is F 18 fluorodeoxyglucose positron emission tomography too sensitive for the diagnosis of vascular endograft infection?
Pamela M Zimmerman, Gregory S Cherr, George C Angelo, et al.
Clinical and Experimental Dermatology
|
September 1, 1994
Dubowitz syndrome with keloidal lesions
M Paradisi, C Angelo, G Conti, et al.
Minerva Pediatrica
|
September 21, 2005
[PTPN11 gene mutation in LEOPARD syndrome]
M Paradisi, C Pedicelli, A Ciasulli, et al.
Clinical and Experimental Dermatology
|
September 3, 2003
Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
M Paradisi, G S Chuang, C Angelo, et al.
Minerva Pediatrica
|
June 23, 2001
[A Pediatric case of lupoid leishmaniasis diagnosed by PCR]
M Paradisi, M G Grosso, C Angelo, et al.
The Journal of Investigative Dermatology
|
March 1, 1995
A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosa
A M Christiano, A Morricone, M Paradisi, et al.
Pediatric Dermatology
|
June 1, 1992
Infantile condylomata of the oral cavity
M Paradisi, S Mostaccioli, G Celano, et al.
Cutis
|
October 1, 1995
Lipoid proteinosis: clinical, histologic, and ultrastructural investigations
A O Muda, M Paradisi, C Angelo, et al.
The Journal of Investigative Dermatology
|
April 1, 1996
A common insertion mutation in COL7A1 in two Italian families with recessive dystrophic epidermolysis bullosa
A M Christiano, M D'Alessio, M Paradisi, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 74) with videos related to
Sort By:
Page
of 8
Minerva Pediatrica
|
May 1, 1997
[Ehlers-Danlos syndrome type I. Ultrastructural study]
M Paradisi, L Giubilei, F Canzona, et al.
Vascular
|
April 7, 2009
Is F 18 fluorodeoxyglucose positron emission tomography too sensitive for the diagnosis of vascular endograft infection?
Pamela M Zimmerman, Gregory S Cherr, George C Angelo, et al.
Clinical and Experimental Dermatology
|
September 1, 1994
Dubowitz syndrome with keloidal lesions
M Paradisi, C Angelo, G Conti, et al.
Minerva Pediatrica
|
September 21, 2005
[PTPN11 gene mutation in LEOPARD syndrome]
M Paradisi, C Pedicelli, A Ciasulli, et al.
Clinical and Experimental Dermatology
|
September 3, 2003
Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
M Paradisi, G S Chuang, C Angelo, et al.
Minerva Pediatrica
|
June 23, 2001
[A Pediatric case of lupoid leishmaniasis diagnosed by PCR]
M Paradisi, M G Grosso, C Angelo, et al.
The Journal of Investigative Dermatology
|
March 1, 1995
A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosa
A M Christiano, A Morricone, M Paradisi, et al.
Pediatric Dermatology
|
June 1, 1992
Infantile condylomata of the oral cavity
M Paradisi, S Mostaccioli, G Celano, et al.
Cutis
|
October 1, 1995
Lipoid proteinosis: clinical, histologic, and ultrastructural investigations
A O Muda, M Paradisi, C Angelo, et al.
The Journal of Investigative Dermatology
|
April 1, 1996
A common insertion mutation in COL7A1 in two Italian families with recessive dystrophic epidermolysis bullosa
A M Christiano, M D'Alessio, M Paradisi, et al.
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of 8