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Pregled bibliografske jedinice broj: 550134

Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction.


Dumic, M; Barisic, N; Rojnic-Putarek, N; Kusec, V; Dumic, K; Huebner, A; Ille, J.
Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction. // 8th Joint meeting of the Lawson Wilkins pediatric endocrine society / European society for pediatric endocrinology
New York, SAD, 2009. str. PO1-023 (poster, međunarodna recenzija, sažetak, znanstveni)


CROSBI ID: 550134 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction.

Autori
Dumic, M ; Barisic, N ; Rojnic-Putarek, N ; Kusec, V ; Dumic, K ; Huebner, A ; Ille, J.

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Skup
8th Joint meeting of the Lawson Wilkins pediatric endocrine society / European society for pediatric endocrinology

Mjesto i datum
New York, SAD, 9-12. rujan 2009

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
triple A syndrome

Sažetak
Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekti:
108-0000000-0359 - Nasljedne endokrine bolesti u djece (Dumić, Miroslav, MZOS ) ( POIROT)
214-1080229-0163 - Zajednička molekularna osnova etiopatogeneza koštanih poremećaja u ljudi (Kušec, Vesna, MZOS ) ( POIROT)

Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb


Citiraj ovu publikaciju:

Dumic, M; Barisic, N; Rojnic-Putarek, N; Kusec, V; Dumic, K; Huebner, A; Ille, J.
Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction. // 8th Joint meeting of the Lawson Wilkins pediatric endocrine society / European society for pediatric endocrinology
New York, SAD, 2009. str. PO1-023 (poster, međunarodna recenzija, sažetak, znanstveni)
Dumic, M., Barisic, N., Rojnic-Putarek, N., Kusec, V., Dumic, K., Huebner, A. & Ille, J. (2009) Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction.. U: 8th Joint meeting of the Lawson Wilkins pediatric endocrine society / European society for pediatric endocrinology.
@article{article, year = {2009}, pages = {PO1-023}, keywords = {triple A syndrome}, title = {Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction.}, keyword = {triple A syndrome}, publisherplace = {New York, SAD} }
@article{article, year = {2009}, pages = {PO1-023}, keywords = {triple A syndrome}, title = {Two siblings with triple A syndrome and novel AAAS mutation presenting as hereditary polyneuropathy due to early neurological dysfunction.}, keyword = {triple A syndrome}, publisherplace = {New York, SAD} }




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