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Pediatric Neurology
|
May 30, 2001
Lack of progression of brain atrophy in Aicardi-Goutières syndrome
A Polizzi, P Pavone, E Parano, et al.
Pediatric Radiology
|
January 1, 1995
Primary osteoma cutis--multiple café-au-lait spots and woolly hair anomaly
M Ruggieri, V Pavone, P Smilari, et al.
European Review for Medical and Pharmacological Sciences
|
December 10, 2014
Otoplasty for prominent ears deformity
P Fioramonti, F Serratore, M Tarallo, et al.
Clinical Dysmorphology
|
November 14, 1997
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism
L Mauceri, M Ruggieri, V Pavone, et al.
Neurology
|
February 1, 1996
Involvement of the white matter in hypomelanosis of Ito (incontinentia pigmenti achromiens)
M Ruggieri, G Tigano, D Mazzone, et al.
European Journal of Pediatrics
|
August 3, 2000
Multiple coronary artery aneurysms in a child with neurofibromatosis type 1
M Ruggieri, G D'Arrigo, M Abbate, et al.
European Review for Medical and Pharmacological Sciences
|
June 21, 2001
Therapeutic approach of carcinoid tumours of the lung
M Ruggieri, F Scocchera, M Genderini, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2005
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly
A Polizzi, P Pavone, P Iannetti, et al.
Postgraduate Medical Journal
|
August 26, 1998
Life-threatening neurological syndrome in Down's syndrome
M Ruggieri, V Pavone, A Polizzi, et al.
American Journal of Medical Genetics
|
January 11, 1996
SHORT syndrome: a new case with probable autosomal dominant inheritance
G Sorge, M Ruggieri, A Polizzi, et al.
Page
of 22
Search research articles
Search
Showing results (51-60 of 220) with videos related to
Sort By:
Page
of 22
Pediatric Neurology
|
May 30, 2001
Lack of progression of brain atrophy in Aicardi-Goutières syndrome
A Polizzi, P Pavone, E Parano, et al.
Pediatric Radiology
|
January 1, 1995
Primary osteoma cutis--multiple café-au-lait spots and woolly hair anomaly
M Ruggieri, V Pavone, P Smilari, et al.
European Review for Medical and Pharmacological Sciences
|
December 10, 2014
Otoplasty for prominent ears deformity
P Fioramonti, F Serratore, M Tarallo, et al.
Clinical Dysmorphology
|
November 14, 1997
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism
L Mauceri, M Ruggieri, V Pavone, et al.
Neurology
|
February 1, 1996
Involvement of the white matter in hypomelanosis of Ito (incontinentia pigmenti achromiens)
M Ruggieri, G Tigano, D Mazzone, et al.
European Journal of Pediatrics
|
August 3, 2000
Multiple coronary artery aneurysms in a child with neurofibromatosis type 1
M Ruggieri, G D'Arrigo, M Abbate, et al.
European Review for Medical and Pharmacological Sciences
|
June 21, 2001
Therapeutic approach of carcinoid tumours of the lung
M Ruggieri, F Scocchera, M Genderini, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2005
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly
A Polizzi, P Pavone, P Iannetti, et al.
Postgraduate Medical Journal
|
August 26, 1998
Life-threatening neurological syndrome in Down's syndrome
M Ruggieri, V Pavone, A Polizzi, et al.
American Journal of Medical Genetics
|
January 11, 1996
SHORT syndrome: a new case with probable autosomal dominant inheritance
G Sorge, M Ruggieri, A Polizzi, et al.
Page
of 22