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Neurology
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September 29, 2004
MRI in acute intermittent maple syrup urine disease
M Di Rocco, R Biancheri, A Rossi, et al.
Clinical Genetics
|
September 12, 2017
Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutation
M Di Rocco, M Rusmini, F Caroli, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Different organic acid patterns in urine and in cerebrospinal fluid in a patient with biotinidase deficiency
M Di Rocco, A Superti-Furga, P Durand, et al.
Pediatric Dermatology
|
February 16, 2007
Unnecessary milk elimination diets in children with atopic dermatitis
J L Sinagra, V Bordignon, C Ferraro, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy
M Di Rocco, L Leveratto, A Cama, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 7, 1999
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly
E Veneselli, R Biancheri, M Di Rocco, et al.
American Journal of Medical Genetics
|
October 1, 1990
Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: report of a second family
M Di Rocco, E Reboa, A Barabino, et al.
AJNR. American Journal of Neuroradiology
|
June 23, 2012
The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a
P Feraco, M Mirabelli-Badenier, M Severino, et al.
Transplantation Proceedings
|
August 19, 2007
Renal allograft immune response is influenced by patient and donor cytokine genotypes
A Canossi, A Piazza, E Poggi, et al.
International Journal of Immunogenetics
|
June 5, 2015
Increased CD1D polymorphism: identification of two novel alleles, CD1D*03 and *04, in individuals from Morocco
A Aureli, K Oumhani, T Del Beato, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 115) with videos related to
Sort By:
Page
of 12
Neurology
|
September 29, 2004
MRI in acute intermittent maple syrup urine disease
M Di Rocco, R Biancheri, A Rossi, et al.
Clinical Genetics
|
September 12, 2017
Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutation
M Di Rocco, M Rusmini, F Caroli, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Different organic acid patterns in urine and in cerebrospinal fluid in a patient with biotinidase deficiency
M Di Rocco, A Superti-Furga, P Durand, et al.
Pediatric Dermatology
|
February 16, 2007
Unnecessary milk elimination diets in children with atopic dermatitis
J L Sinagra, V Bordignon, C Ferraro, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1993
Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy
M Di Rocco, L Leveratto, A Cama, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 7, 1999
Unusually prolonged survival and childhood-onset epilepsy in a case of alobar holoprosencephaly
E Veneselli, R Biancheri, M Di Rocco, et al.
American Journal of Medical Genetics
|
October 1, 1990
Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: report of a second family
M Di Rocco, E Reboa, A Barabino, et al.
AJNR. American Journal of Neuroradiology
|
June 23, 2012
The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a
P Feraco, M Mirabelli-Badenier, M Severino, et al.
Transplantation Proceedings
|
August 19, 2007
Renal allograft immune response is influenced by patient and donor cytokine genotypes
A Canossi, A Piazza, E Poggi, et al.
International Journal of Immunogenetics
|
June 5, 2015
Increased CD1D polymorphism: identification of two novel alleles, CD1D*03 and *04, in individuals from Morocco
A Aureli, K Oumhani, T Del Beato, et al.
Page
of 12