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Human Genetics
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March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
Ferdinanda Annesi, E F Rocca, I C Cirò Candiano, et al.
Human Genetics
|
March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
Innocenza Claudia Cirò Candiano, F Annesi, E F Rocca, et al.
Veterinary Journal (London, England : 1997)
|
May 22, 2024
Evaluation of coagulation profile in dogs with ACTH-dependent hyperadrenocorticism compared to healthy dogs by rotational thromboelastometry (ROTEM)
F G Romão, B Dos Santos, S E V Mora, et al.
Epilepsy Research
|
February 28, 2007
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy
Elvira V De Marco, Antonio Gambardella, Ferdinanda Annesi, et al.
Journal of Neurology
|
December 18, 2007
Hyperhomocysteinemia is associated with cognitive impairment in multiple sclerosis
C Russo, F Morabito, F Luise, et al.
Journal of Neurology
|
January 13, 2000
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension
A Quattrone, A Gambardella, A M Carbone, et al.
Molecular Psychiatry
|
June 7, 2017
Rescue of impaired sociability and anxiety-like behavior in adult cacna1c-deficient mice by pharmacologically targeting eIF2α
Z D Kabir, A Che, D K Fischer, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy
Giovanni Provenzano, E Mannarino, F Annesi, et al.
European Review for Medical and Pharmacological Sciences
|
May 13, 2014
Densitometric kneecap changes after unilateral knee arthroplasty
F Barchetti, A Stagnitti, N Al Ansari, et al.
Clinical Genetics
|
September 14, 2007
Gene dosage influences the age at onset of SCA2 in a family from southern Italy
P Spadafora, G Annesi, M Liguori, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 84) with videos related to
Sort By:
Page
of 9
Human Genetics
|
March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
Ferdinanda Annesi, E F Rocca, I C Cirò Candiano, et al.
Human Genetics
|
March 20, 2008
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease
Innocenza Claudia Cirò Candiano, F Annesi, E F Rocca, et al.
Veterinary Journal (London, England : 1997)
|
May 22, 2024
Evaluation of coagulation profile in dogs with ACTH-dependent hyperadrenocorticism compared to healthy dogs by rotational thromboelastometry (ROTEM)
F G Romão, B Dos Santos, S E V Mora, et al.
Epilepsy Research
|
February 28, 2007
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy
Elvira V De Marco, Antonio Gambardella, Ferdinanda Annesi, et al.
Journal of Neurology
|
December 18, 2007
Hyperhomocysteinemia is associated with cognitive impairment in multiple sclerosis
C Russo, F Morabito, F Luise, et al.
Journal of Neurology
|
January 13, 2000
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension
A Quattrone, A Gambardella, A M Carbone, et al.
Molecular Psychiatry
|
June 7, 2017
Rescue of impaired sociability and anxiety-like behavior in adult cacna1c-deficient mice by pharmacologically targeting eIF2α
Z D Kabir, A Che, D K Fischer, et al.
Human Genetics
|
August 21, 2009
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy
Giovanni Provenzano, E Mannarino, F Annesi, et al.
European Review for Medical and Pharmacological Sciences
|
May 13, 2014
Densitometric kneecap changes after unilateral knee arthroplasty
F Barchetti, A Stagnitti, N Al Ansari, et al.
Clinical Genetics
|
September 14, 2007
Gene dosage influences the age at onset of SCA2 in a family from southern Italy
P Spadafora, G Annesi, M Liguori, et al.
Page
of 9