\u3cp\u3eBACKGROUND: Pyridoxine dependent epilepsy is a rare cause of seizures in childhood. The diagnosis is made on clinical criteria, that in many cases are never met. Therefore, epidemiological data on pyridoxine dependency are scarce.\u3c/p\u3e\u3cp\u3eAIMS: To study the epidemiology of pyridoxine dependent epilepsy in the Netherlands, and to determine whether the diagnosis is based on the appropriate criteria.\u3c/p\u3e\u3cp\u3eMETHODS: Nationwide all departments of paediatrics (n = 113) and of paediatric or neonatal neurology (n = 17) were asked to report cases of pyridoxine dependent seizures. Birth incidences were calculated using national data on live births from 1991 to 2003.\u3c/p\u3e\u3cp\u3eRESULTS: Response was received from ...
BACKGROUND: Pyridoxine-dependent seizures (PDS) is a rare, autosomal recessively inherited disorder....
Gül-Mert G, İncecik F, Hergüner Mö, Ceylaner S, Altunbaşak Ş. Pyridoxine-dependent epilepsy in two T...
International audiencePyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive metabolic di...
Item does not contain fulltextBACKGROUND: Pyridoxine dependent epilepsy is a rare cause of seizures ...
AIM: The long-term outcome of the Dutch pyridoxine-dependent epilepsy cohort and correlations betwee...
The aim of our study was to describe the clinical, electroencephalogram, molecular findings and the ...
Eight children with pyridoxine-dependent seizures (PDS) were seen over a period of 10 years. Of thos...
Item does not contain fulltextAim The long-term outcome of the Dutch pyridoxine-dependent epilepsy c...
Background: Little is known about pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde de...
The aim of our study was to describe the clinical, electroencephalogram, molecular findings and the ...
Abstract Pyridoxine dependent epilepsies (PDEs) are rare autosomal recessive disorders with onset in...
Pyridoxine dependent epilepsies (PDEs) are rare autosomal recessive disorders with onset in neonatal...
Contains fulltext : 112902.pdf (publisher's version ) (Open Access)Radboud Univers...
Aim: In pyridoxine dependent epilepsy (PDE), patients usually present with neonatal seizures. Receiv...
Aim: In pyridoxine dependent epilepsy (PDE), patients usually present with neonatal seizures. Receiv...
BACKGROUND: Pyridoxine-dependent seizures (PDS) is a rare, autosomal recessively inherited disorder....
Gül-Mert G, İncecik F, Hergüner Mö, Ceylaner S, Altunbaşak Ş. Pyridoxine-dependent epilepsy in two T...
International audiencePyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive metabolic di...
Item does not contain fulltextBACKGROUND: Pyridoxine dependent epilepsy is a rare cause of seizures ...
AIM: The long-term outcome of the Dutch pyridoxine-dependent epilepsy cohort and correlations betwee...
The aim of our study was to describe the clinical, electroencephalogram, molecular findings and the ...
Eight children with pyridoxine-dependent seizures (PDS) were seen over a period of 10 years. Of thos...
Item does not contain fulltextAim The long-term outcome of the Dutch pyridoxine-dependent epilepsy c...
Background: Little is known about pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde de...
The aim of our study was to describe the clinical, electroencephalogram, molecular findings and the ...
Abstract Pyridoxine dependent epilepsies (PDEs) are rare autosomal recessive disorders with onset in...
Pyridoxine dependent epilepsies (PDEs) are rare autosomal recessive disorders with onset in neonatal...
Contains fulltext : 112902.pdf (publisher's version ) (Open Access)Radboud Univers...
Aim: In pyridoxine dependent epilepsy (PDE), patients usually present with neonatal seizures. Receiv...
Aim: In pyridoxine dependent epilepsy (PDE), patients usually present with neonatal seizures. Receiv...
BACKGROUND: Pyridoxine-dependent seizures (PDS) is a rare, autosomal recessively inherited disorder....
Gül-Mert G, İncecik F, Hergüner Mö, Ceylaner S, Altunbaşak Ş. Pyridoxine-dependent epilepsy in two T...
International audiencePyridoxine-dependent epilepsy (PDE) is a rare autosomal recessive metabolic di...