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Neuropsihijatrija
|
January 1, 1975
[Echoencephalography as a diagnostic procedure in epilepsy]
N Gubarev, N Zurak, F Hajnsek
The Journal of International Medical Research
|
January 1, 1989
Intravenous chlormethiazole in the management of primary trigeminal neuralgia resistant to conventional therapy
N Zurak, B Randic, Z Poljaković, et al.
Neuropsihijatrija
|
January 1, 1976
[Analysis of epileptic seizures in acute cerebrovascular attacks]
B Barac, D Bozicević, N Zurak, et al.
Neurologia Croatica : Glasilo Udruzenja Neurologa Jugoslavije = Official Journal of Yugoslav Neurological Association
|
January 1, 1991
Epileptic seizures as a symptom of various neurological diseases
V Brinar, D Bozicević, N Zurak, et al.
Acta Medica Iugoslavica
|
January 1, 1977
A critical review of cerebrospinal fluid analyses in patients with acute cerebrovascular accident. A biochemical and clinicopathological study
K Arko, N Zurak, V Hlavka, et al.
Age and Ageing
|
September 14, 2000
Spontaneous rupture of oesophagus (Boerhaave's syndrome) related to rivastigmine
T Babic, L Banfic, J Papa, et al.
European Journal of Neurology
|
November 23, 2006
Comparison of the growth hormone, IGF-1 and insulin in cerebrospinal fluid and serum between patients with motor neuron disease and healthy controls
E Bilic, E Bilic, I Rudan, et al.
Advances in Medical Sciences
|
November 27, 2013
The dynamics of soluble Fas/APO 1 apoptotic biochemical marker in acute ischemic stroke patients
D Mahovic, N Zurak, N Lakusic, et al.
Croatian Medical Journal
|
November 7, 2000
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
N Canki-Klain, D Récan, D Milicić, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 11, 2005
Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants
N Barisic, J S Müller, E Paucic-Kirincic, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Neuropsihijatrija
|
January 1, 1975
[Echoencephalography as a diagnostic procedure in epilepsy]
N Gubarev, N Zurak, F Hajnsek
The Journal of International Medical Research
|
January 1, 1989
Intravenous chlormethiazole in the management of primary trigeminal neuralgia resistant to conventional therapy
N Zurak, B Randic, Z Poljaković, et al.
Neuropsihijatrija
|
January 1, 1976
[Analysis of epileptic seizures in acute cerebrovascular attacks]
B Barac, D Bozicević, N Zurak, et al.
Neurologia Croatica : Glasilo Udruzenja Neurologa Jugoslavije = Official Journal of Yugoslav Neurological Association
|
January 1, 1991
Epileptic seizures as a symptom of various neurological diseases
V Brinar, D Bozicević, N Zurak, et al.
Acta Medica Iugoslavica
|
January 1, 1977
A critical review of cerebrospinal fluid analyses in patients with acute cerebrovascular accident. A biochemical and clinicopathological study
K Arko, N Zurak, V Hlavka, et al.
Age and Ageing
|
September 14, 2000
Spontaneous rupture of oesophagus (Boerhaave's syndrome) related to rivastigmine
T Babic, L Banfic, J Papa, et al.
European Journal of Neurology
|
November 23, 2006
Comparison of the growth hormone, IGF-1 and insulin in cerebrospinal fluid and serum between patients with motor neuron disease and healthy controls
E Bilic, E Bilic, I Rudan, et al.
Advances in Medical Sciences
|
November 27, 2013
The dynamics of soluble Fas/APO 1 apoptotic biochemical marker in acute ischemic stroke patients
D Mahovic, N Zurak, N Lakusic, et al.
Croatian Medical Journal
|
November 7, 2000
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
N Canki-Klain, D Récan, D Milicić, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 11, 2005
Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants
N Barisic, J S Müller, E Paucic-Kirincic, et al.
Page
of 3