Dear Ciaran,
I'm not from JabRef team, but try to answer: the fragment you've tried to
import id not BibTeX, it is likelyto be RIS, with some extra text in
beginning. Probably, that's the matter.
Unfortunately, I've never worked with OVID and have no access to it.
Note: JabRef stored its data in BibTeX.
Regards,
Nikolay
2011/7/27 Ciarán Clarke <[email protected]>
> Dear Sir or Madam,
>
> When I try to import a file in any of the above formats, none of the
> filters is recognised ('No entries Please make sure you are using the
> correct import filter'). If I import using 'all files', al fields are
> correctly imported except the author field
>
> In BibTex format, a sample citation
> Version:1.0 StartHTML:0000000167 EndHTML:0000004268
> StartFragment:0000000503 EndFragment:0000004252
> TY - GEN
> A1 - Alpman A.
> A1 - Serdaroglu G.
> A1 - Cogulu O.
> A1 - Tekgul H.
> A1 - Gokben S.
> A1 - ,Ozkinay F.
> T1 - Ring chromosome 20 syndrome with intractable epilepsy
> T2 - Developmental Medicine and Child Neurology JA - Dev. Med. Child
> Neurol.
> Y1 - 2005///
> VL - 47
> IS - 5
> SP - 343
> EP - 346
> KW - adolescent
> KW - aggressiveness
> KW - article
> KW - automutilation
> KW - behavior disorder
> KW - *benign childhood epilepsy/di [Diagnosis]
> KW - *benign childhood epilepsy/dt [Drug Therapy]
> KW - *benign childhood epilepsy/su [Surgery]
> KW - *benign childhood epilepsy/th [Therapy]
> KW - case report
> KW - *chromosome 20
> KW - clinical feature
> KW - corpus callosum transsection
> KW - disease association
> KW - disease severity
> KW - ear malformation
> KW - electroencephalography
> KW - eyelid disease
> KW - face dysmorphia
> KW - follow up
> KW - human
> KW - *intractable epilepsy/di [Diagnosis]
> KW - *intractable epilepsy/dt [Drug Therapy]
> KW - *intractable epilepsy/su [Surgery]
> KW - *intractable epilepsy/th [Therapy]
> KW - karyotyping
> KW - learning disorder
> KW - male
> KW - microcephaly
> KW - micrognathia
> KW - nerve stimulation
> KW - priority journal
> KW - *ring chromosome/di [Diagnosis]
> KW - strabismus
> KW - vagus nerve
> KW - carbamazepine/dt [Drug Therapy]
> KW - corticotropin/dt [Drug Therapy]
> KW - gabapentin/dt [Drug Therapy]
> KW - immunoglobulin/dt [Drug Therapy]
> KW - immunoglobulin/iv [Intravenous Drug Administration]
> KW - lamotrigine/dt [Drug Therapy]
> KW - valproic acid/dt [Drug Therapy]
> KW - vigabatrin/dt [Drug Therapy]
> CY - United Kingdom
> SN - 0012-1622
> AB - Ring chromosome 20 (r[20]) syndrome is characterized by mild to
> moderate learning disability*, behavioural disorders, epilepsy, and various
> dysmorphic features. Although still considered rare, r (20) syndrome is
> being increasingly diagnosed. More than 30 cases have been described in the
> literature since 1976. Here we report an additional case of a 14-year-old
> male with r (20). He had moderate to severe learning disability and
> epileptic seizures manifesting at about 18 months of age. During the 13
> years' follow-up period he showed intractable epileptic seizures,
> behavioural disorders, and mild dysmorphological features including
> microcephaly, strabismus, micrognathia, down-slanting eyelids, and ear
> abnormalities. Frequent episodes of atypical absence or non-convulsive
> status associated with electroencephalogram changes were seen in follow-up.
> He was treated with several classical and new antiepileptic drugs, including
> intravenous immunoglobulin, corticotropin, and vagal nerve stimulation, with
> unsuccessful control of seizures. Finally, surgical treatment (corpus
> callosotomy) was performed at the age of 13 years; severity of tonic
> seizures was diminished, but frequency was unchanged. Although his
> behavioural problems, e.g. hyperactivity, were mild in early childhood they
> became more severe when he was 11 years old. Aggressiveness, compulsiveness
> with self-injury, and panic attacks developed at the age of 13 years, and
> were more pronounced after callosotomy. This case report provides the first
> description of deterioration in psychological situation in patients with r
> (20) intractable epilepsy. The patient was diagnosed with r (20) syndrome
> after 13 years of clinical follow-up. Karyotype analysis should, therefore,
> be performed in every patient with intractable epilepsy of unknown
> aetiology.
> N1 - Date of Input: 7/27/2011
> N1 - Priority: Normal
> N1 - A. Alpman, Ege University Medical Faculty, Department of Paediatrics,
> 35 100 Bornova-Izmir, Turkey. E-mail: [email protected]
> L1 -
> http://ovidsp.ovid.com/ovidweb.cgi?T=JS&PAGE=reference&D=emed7&NEWS=N&AN=2005215483
>
> ER -
>
> In Jabref, the imported citation contains, in the author field, only 'A. et
> al.'.
>
> The source of the references is OVID. I have imported other references from
> EBSCOhost without difficulty.
>
> I'm afraid I'm unable to tinker with import filters, and I would suggest any
> advice you could give. I've checked the users' forum without success.
>
> Many thanks for a great product.
>
> Ciaran Clarke
>
>
>
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