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Journal of Neurology, Neurosurgery, and Psychiatry
|
February 18, 2003
Chiari I malformation mimicking myasthenia gravis
C Rodolico, P Girlanda, C Nicolosi, et al.
Journal of the American Society of Nephrology : JASN
|
March 12, 1999
Prevalence and clinical outcome associated with preexisting malnutrition in acute renal failure: a prospective cohort study
E Fiaccadori, M Lombardi, S Leonardi, et al.
Minerva Pediatrica
|
November 30, 1982
[The Sotos syndrome in 2 brothers. Confirmation of a recessive autosomal heredity?]
M Gemelli, N Carlo Stella, G Barberio, et al.
Neurology
|
March 27, 2002
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene
F Moro, R Carrozzo, P Veggiotti, et al.
European Journal of Neurology
|
June 26, 2003
Highly disabling cerebellar presentation in Huntington disease
F Squitieri, G Pustorino, M Cannella, et al.
Clinical Genetics
|
October 9, 2012
Early-onset epileptic encephalopathy in a girl carrying a truncating mutation of the ARX gene: rethinking the ARX phenotype in females
E Bettella, G Di Rosa, R Polli, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 8, 1999
Diagnostic and prognostic value of vasodilator stress echocardiography in asymptomatic Type 2 diabetic patients with positive exercise thallium scintigraphy: a pilot study
O Gaddi, G Tortorella, E Picano, et al.
Chest
|
December 1, 1994
Hemodynamic, respiratory, and metabolic effects of medium-chain triglyceride-enriched lipid emulsions following valvular heart surgery
E Fiaccadori, G Tortorella, G Gonzi, et al.
Minerva Pediatrica
|
July 13, 2006
[Neurobiology of autism: Study of a sample of autistic children]
E Germanò, A Gagliano, A Magazù, et al.
Neurology
|
February 7, 2007
Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia
D Mei, E Parrini, M Pasqualetti, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 35) with videos related to
Sort By:
Page
of 4
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 18, 2003
Chiari I malformation mimicking myasthenia gravis
C Rodolico, P Girlanda, C Nicolosi, et al.
Journal of the American Society of Nephrology : JASN
|
March 12, 1999
Prevalence and clinical outcome associated with preexisting malnutrition in acute renal failure: a prospective cohort study
E Fiaccadori, M Lombardi, S Leonardi, et al.
Minerva Pediatrica
|
November 30, 1982
[The Sotos syndrome in 2 brothers. Confirmation of a recessive autosomal heredity?]
M Gemelli, N Carlo Stella, G Barberio, et al.
Neurology
|
March 27, 2002
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene
F Moro, R Carrozzo, P Veggiotti, et al.
European Journal of Neurology
|
June 26, 2003
Highly disabling cerebellar presentation in Huntington disease
F Squitieri, G Pustorino, M Cannella, et al.
Clinical Genetics
|
October 9, 2012
Early-onset epileptic encephalopathy in a girl carrying a truncating mutation of the ARX gene: rethinking the ARX phenotype in females
E Bettella, G Di Rosa, R Polli, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
October 8, 1999
Diagnostic and prognostic value of vasodilator stress echocardiography in asymptomatic Type 2 diabetic patients with positive exercise thallium scintigraphy: a pilot study
O Gaddi, G Tortorella, E Picano, et al.
Chest
|
December 1, 1994
Hemodynamic, respiratory, and metabolic effects of medium-chain triglyceride-enriched lipid emulsions following valvular heart surgery
E Fiaccadori, G Tortorella, G Gonzi, et al.
Minerva Pediatrica
|
July 13, 2006
[Neurobiology of autism: Study of a sample of autistic children]
E Germanò, A Gagliano, A Magazù, et al.
Neurology
|
February 7, 2007
Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia
D Mei, E Parrini, M Pasqualetti, et al.
Page
of 4