Results 101 to 110 of about 557 (135)
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Genetika afektivnih poremećaja
2006Vjeruje se da su afektivni poremećaji uzrokovani većim brojem gena s malim efektom čija ekspresija ovisi o faktorima okoline Afektivni poremećaji spadaju u složene genske poremećaje, a to znači da se poremećaj ne može pripisati pojedinačnim dominantnim ili recesivnim genima u općoj populaciji.
Štrkalj-Ivezić, Slađana +6 more
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2019
Hipofizės adenomos yra gėrybiniai priekinės hipofizės dalies augliai. Radiolginių ir autopsijų studijų duomenimis, hipofizės adenomos yra gana dažnos, nustatomos 15-20 proc. žmonių. Tai trečias pagal dažnį intrakranijinis auglys po meningiomų ir gliomų. Hipofizės adenomos 95 proc.
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Hipofizės adenomos yra gėrybiniai priekinės hipofizės dalies augliai. Radiolginių ir autopsijų studijų duomenimis, hipofizės adenomos yra gana dažnos, nustatomos 15-20 proc. žmonių. Tai trečias pagal dažnį intrakranijinis auglys po meningiomų ir gliomų. Hipofizės adenomos 95 proc.
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2007
U odlomku su opisane dosadašnje spoznaje o nasljednoj osnovi psihijatrijskih bolesti, metodologija genetičkih istraživanja, prikazan je pregled genskih polimorfizama koji se povezuju s pojavom različitih psihijatrijskih bolesti, te je opisano značenje farmakogenomike u psihijatriji.
openaire
U odlomku su opisane dosadašnje spoznaje o nasljednoj osnovi psihijatrijskih bolesti, metodologija genetičkih istraživanja, prikazan je pregled genskih polimorfizama koji se povezuju s pojavom različitih psihijatrijskih bolesti, te je opisano značenje farmakogenomike u psihijatriji.
openaire
2012
The most common form of monogenic diabetes is MODY (Maturity-Onset Diabetes of the Young). It ranks among genetic defects of the β cell. It is clinically heterogenous group of disorders characterised with non insulin-dependent diabetes mellitus with autosomal dominant inheritance and age at diagnosis up to 40 years.
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The most common form of monogenic diabetes is MODY (Maturity-Onset Diabetes of the Young). It ranks among genetic defects of the β cell. It is clinically heterogenous group of disorders characterised with non insulin-dependent diabetes mellitus with autosomal dominant inheritance and age at diagnosis up to 40 years.
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ALGORITMA EVOLUSI GENETIKA SEBAGAI FUNGSI OPTIMASI JARINGAN SARAF BUATAN
Device, 2021Muhamad Fuat Asnawi
exaly
Miskonsepsi Materi Genetika tentang Ekspresi Gen
BIOEDUSAINS: Jurnal Pendidikan Biologi Dan Sains, 2020Tomi Hidayat
exaly
2018
Chromosome 21 is autosomal and acrocentric chromosome whose full or partial aneuploidy causes pathological changes in the carrier phenotype. Among the many types of aberrations, dominate standard trisomy 21, known as Down syndrome. This disorder also occurs as a result of duplication, deletion and translocation in the genome or as a result of the ...
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Chromosome 21 is autosomal and acrocentric chromosome whose full or partial aneuploidy causes pathological changes in the carrier phenotype. Among the many types of aberrations, dominate standard trisomy 21, known as Down syndrome. This disorder also occurs as a result of duplication, deletion and translocation in the genome or as a result of the ...
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Genetika psychických onemocnění
2019Psychological diseases are very heterogeneus group of diseases, including a complicated and complex multifactorial etiology with a possibility of an important role of a genetic component. Some diaseses got discovered their clear genetic origins, for instance Rett syndrom, where the origins are caused by a mutation in gen MECP2.
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Molekularna forenzična genetika
2009IZVOD IZ RECENZIJE Tekst obuhvata aktualne sadržaje koji su detaljno i zanimljivo prezentirani. Dosljedno elaborirajući moderan i inovativan pristup autori nas upoznaju sa osnovnim parametrima molekularne forenzične genetike, kako u sferi njenih znanstvenih temelja tako i u oblasti njene konkretne primjene.
Primorac, Dragan, Marjanović, Damir
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Genetics of Alzheimer's Disease in Clinical Practice
Neurologie Pro Praxi, 2019Martin Vyhnálek, Jan Laczo
exaly