About: Mohamad A. Mikati

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl) طبيب وأستاذ جامعي لبناني (ar)
rdfs:label	Mohamad A. Mikati (en) Mohamad A. Mikati (es) Mohamad A. Mikati (nl) Mohamad A. Mikati (sl) Mohamad A. Mikati (ast) محمد ميقاتي (ar)
skos:prefLabel	Mohamad A. Mikati (en) Mohamad A. Mikati (es) Mohamad A. Mikati (nl) Mohamad A. Mikati (sl) Mohamad A. Mikati (ast) محمد ميقاتي (ar)
name	Mohamad A. Mikati (en) Mohamad A. Mikati (es) Mohamad A. Mikati (nl) Mohamad A. Mikati (sl) Mohamad A. Mikati (ast) محمد ميقاتي (ar)
LinkedIn personal profile ID	wds:Q44880597-e8675203-4714-dd99-2ccf-ce9d187594ca
LinkedIn personal profile ID	mohamad-mikati-68495714
Scopus author ID	wds:Q44880597-B60ED534-2733-4C5F-BAC1-8C54520A1B4F
Scopus author ID	7005469208
given name	wds:Q44880597-325b5cae-435d-2435-01d1-4a306f89e76e
given name	Mohamad
instance of	wds:Q44880597-00E50AE1-2F0B-4725-99F4-C19C53B00327
instance of	Homo sapiens
Google Scholar author ID	wds:Q44880597-e34dff26-4a05-918f-0320-5ea08e9cc4b3
Google Scholar author ID	uYs0Y2sAAAAJ
skos:altLabel	Mikati, Mohamad (en) Mikati, Mohamad A. (en) Mohamad Abdul Mikati (en) Mohamad Mikati (en)
native language	wds:Q44880597-ded1db9c-4b16-be94-9396-9c3aabed211e
occupation	wds:Q44880597-8dcab81b-474a-6cde-218c-0efc2d220a54 wds:Q44880597-e79ece3c-4ba5-ccdd-cd23-f57f3f699c13
employer	wds:Q44880597-B3A147F1-4D75-4B4B-8E7A-D63555988C88
languages spoken, written or signed	wds:Q44880597-3cb0133b-4cfd-6171-41c7-63bfd4da723d wds:Q44880597-6e1f4999-4760-9f31-b344-e5787f64a0ec
name in native language	wds:Q44880597-d0f797ab-418f-8979-5cdc-9963ec529c21
sex or gender	wds:Q44880597-C6221921-33E4-433C-A983-B23912B39FEA
ISNI	wds:Q44880597-b02aa234-4535-fb7c-49cc-2efabd720ac2
VIAF ID	wds:Q44880597-2ea4487a-442f-758f-a9ab-a11270462d16
Library of Congress authority ID	wds:Q44880597-a7d9ea4d-4dac-3325-f798-00865a1889f6
country of citizenship	wds:Q44880597-3332949b-4d0a-12d6-9b74-d5f556bd90bb
RERO ID (obsolete)	wds:Q44880597-a6fb04cf-492d-1fc4-5d9f-c949188955d9
educated at	wds:Q44880597-4b0df73b-4815-7c8d-8f0f-f1abaa7fa571 wds:Q44880597-4dae1ccc-4e03-6f90-7624-5a4a1edf5bf3 wds:Q44880597-4e981775-49ae-e908-4c3c-a9d4b2e40537
family name	wds:Q44880597-6fb60973-4e95-95cd-4e99-2d61dbaa3228
Canadiana Name Authority ID	wds:Q44880597-378d621a-4871-7aaa-6ff1-d114cda39292
National Library of Israel J9U ID	wds:Q44880597-4f0edaa1-4f38-c395-07fc-05c989b01e5c
VIAF ID	http://viaf.org/viaf/305025384
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2013184683
native language	Arabic
occupation	university teacher physician
employer	Duke University
languages spoken, written or signed	Arabic English
name in native language	مُحمَّد ميقاتي (ar)
sex or gender	male
ISNI	0000000417045184
VIAF ID	305025384
Library of Congress authority ID	n2013184683
country of citizenship	Lebanon
RERO ID (obsolete)	02-A023678324
educated at	Harvard University American University of Beirut
family name	Mikati
Canadiana Name Authority ID	ncf11617416
National Library of Israel J9U ID	987007374478205171
ORCID iD	wds:Q44880597-E5899406-CA80-42DE-946B-EF3BA788F0E2
ORCID iD	https://orcid.org/0000-0003-0363-8715
ORCID iD	0000-0003-0363-8715
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q44880597
is author of	Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients Brain malformation and infantile spasms in a SCAD deficiency patient. Pyridoxine-dependent epilepsy: EEG investigations and long-term follow-up Distinct neurological disorders with ATP1A3 mutations Behavioral side effects of gabapentin in children. Changes in sphingomyelinases, ceramide, Bax, Bcl(2), and caspase-3 during and after experimental status epilepticus Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes Functional recovery following resection of an epileptogenic focus in the motor hand area Biotin-responsive basal ganglia disease: case report and review of the literature.

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