cholecalciferol and Epilepsy--Tonic-Clonic

cholecalciferol has been researched along with Epilepsy--Tonic-Clonic* in 2 studies

Other Studies

2 other study(ies) available for cholecalciferol and Epilepsy--Tonic-Clonic

Article	Year
An unusual case of paroxysmal kinesigenic dyskinesia. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2002, Volume: 9, Issue:1 Paroxysmal kinesigenic dyskinesia (PKD) is an uncommon neurological disorder characterised by abnormal episodic brief movements induced by sudden movements of the body. The recognition and understanding of this disorder has increased over the past few decades. While most cases are idiopathic, the association of PKD with various disorders, including metabolic abnormalities has also been reported. We report an interesting case of a 52 year old male who presented with PKD manifesting as subtle facio-brachial movements and apraxia of eyelid opening (ALO) secondary toidiopathic hypoparathyroidism. Topics: Arm; Brain Diseases; Calcinosis; Calcium Carbonate; Cholecalciferol; Chorea; Epilepsy, Tonic-Clonic; Eyelids; Facial Muscles; Humans; Hypoparathyroidism; Male; Middle Aged; Movement; Shoulder	2002
[Severe rachitic osteopathy during long-term anticonvulsant treatment]. Deutsche medizinische Wochenschrift (1946), 1973, May-18, Volume: 98, Issue:20 Topics: Administration, Oral; Alkaline Phosphatase; Anticonvulsants; Biopsy; Calcium; Carbamazepine; Child; Cholecalciferol; Epilepsy, Tonic-Clonic; Humans; Ilium; Iron; Long-Term Care; Male; Osteomalacia; Phenobarbital; Phenytoin; Phosphorus; Primidone; Rickets	1973

Article

Year

An unusual case of paroxysmal kinesigenic dyskinesia.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2002, Volume: 9, Issue:1

Paroxysmal kinesigenic dyskinesia (PKD) is an uncommon neurological disorder characterised by abnormal episodic brief movements induced by sudden movements of the body. The recognition and understanding of this disorder has increased over the past few decades. While most cases are idiopathic, the association of PKD with various disorders, including metabolic abnormalities has also been reported. We report an interesting case of a 52 year old male who presented with PKD manifesting as subtle facio-brachial movements and apraxia of eyelid opening (ALO) secondary toidiopathic hypoparathyroidism.

Topics: Arm; Brain Diseases; Calcinosis; Calcium Carbonate; Cholecalciferol; Chorea; Epilepsy, Tonic-Clonic; Eyelids; Facial Muscles; Humans; Hypoparathyroidism; Male; Middle Aged; Movement; Shoulder

2002

[Severe rachitic osteopathy during long-term anticonvulsant treatment].

Deutsche medizinische Wochenschrift (1946), 1973, May-18, Volume: 98, Issue:20

Topics: Administration, Oral; Alkaline Phosphatase; Anticonvulsants; Biopsy; Calcium; Carbamazepine; Child; Cholecalciferol; Epilepsy, Tonic-Clonic; Humans; Ilium; Iron; Long-Term Care; Male; Osteomalacia; Phenobarbital; Phenytoin; Phosphorus; Primidone; Rickets

1973