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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1993
Diagnosis of neurofibromatosis type 1 using RFLPs tightly linked to gene
R Vivarelli, G Bartalani, A Berardi, et al.
Clinical EEG (Electroencephalography)
|
April 1, 1988
Intractable epilepsy: etiology, risk factors and treatment
A Fois, D Tomaccini, P Balestri, et al.
Brain & Development
|
January 9, 2007
Aicardi syndrome with favorable outcome: case report and review
S Grosso, G Lasorella, A Russo, et al.
Human Genetics
|
December 29, 2000
Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene
R Sestini, R Vivarelli, P Balestri, et al.
Neurology
|
August 8, 2007
SCN1A mutation associated with atypical Panayiotopoulos syndrome
S Grosso, A Orrico, L Galli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 1, 1992
Biochemical diagnosis of Canavan disease
G Bartalini, M Margollicci, P Balestri, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
July 13, 2001
Pubertal disorders in inv dup(15) syndrome
S Grosso, P Balestri, C Anichini, et al.
Brain & Development
|
February 28, 2001
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria
R Vivarelli, S Grosso, M Cioni, et al.
Neurosurgery
|
February 16, 2002
Association of Chiari I malformation, mental retardation, speech delay, and epilepsy: a specific disorder?
S Grosso, R Scattolini, G Paolo, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 1, 1993
Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1
P Balestri, L Calistri, R Vivarelli, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 64) with videos related to
Sort By:
Page
of 7
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1993
Diagnosis of neurofibromatosis type 1 using RFLPs tightly linked to gene
R Vivarelli, G Bartalani, A Berardi, et al.
Clinical EEG (Electroencephalography)
|
April 1, 1988
Intractable epilepsy: etiology, risk factors and treatment
A Fois, D Tomaccini, P Balestri, et al.
Brain & Development
|
January 9, 2007
Aicardi syndrome with favorable outcome: case report and review
S Grosso, G Lasorella, A Russo, et al.
Human Genetics
|
December 29, 2000
Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene
R Sestini, R Vivarelli, P Balestri, et al.
Neurology
|
August 8, 2007
SCN1A mutation associated with atypical Panayiotopoulos syndrome
S Grosso, A Orrico, L Galli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 1, 1992
Biochemical diagnosis of Canavan disease
G Bartalini, M Margollicci, P Balestri, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
July 13, 2001
Pubertal disorders in inv dup(15) syndrome
S Grosso, P Balestri, C Anichini, et al.
Brain & Development
|
February 28, 2001
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria
R Vivarelli, S Grosso, M Cioni, et al.
Neurosurgery
|
February 16, 2002
Association of Chiari I malformation, mental retardation, speech delay, and epilepsy: a specific disorder?
S Grosso, R Scattolini, G Paolo, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 1, 1993
Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1
P Balestri, L Calistri, R Vivarelli, et al.
Page
of 7