Results 31 to 40 of about 5,862 (302)

Aging Is a Key Driver for Adult Acute Myeloid Leukemia

open access: yesAging and Cancer, EarlyView.
Acute myeloid leukemia (AML) is a classical age‐related hematologic malignancy, and a key driver of AML is aging, which profoundly regulates intrinsic factors such as genomic instability, epigenetic reprogramming, and metabolic dysregulation, and alters bone marrow microenvironment.
Rong Yin, Haojian Zhang
wiley   +1 more source

Impact of the EU Succession Regulation on Statutory Inheritance [PDF]

open access: yes, 2018
The new EU Succession Regulation has caused a series of controversies. Doubts are linked, inter alia, to the application, as a result of the Regulation, of national laws, which in many places differ from each other. One such area is statutory inheritance.
Załucki, Mariusz   +2 more
core   +2 more sources

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

The Certificate of Inheritance – Legal Nature and Probative Value

open access: yesBulletin of the Transilvania University of Braşov: Series VII: Social Sciences, Law, 2022
The certificate of inheritance is the final act of the notary succession procedure which serves as proof of quality of heir and the property right of the accepted heirs over the goods of the successor mass, in the amount awarded to each heir. Doctrine
Diana G. Ionas
doaj   +1 more source

Gift-giving and inheritance strategies in late Roman law and legal practice [PDF]

open access: yes, 2017
In Roman law, an inheritance could be passed on according to the rules of intestate or testate succession. The Roman law of succession presents people with an enormous display of legal ingenuity.
Caroline Humfress, Humfress, Caroline
core   +1 more source

Value of MRI Outcomes for Preventive and Early‐Stage Trials in Spinocerebellar Ataxias 1 and 3

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To examine the value of MRI outcomes as endpoints for preventive and early‐stage trials of two polyglutamine spinocerebellar ataxias (SCAs). Methods A cohort of 100 participants (23 SCA1, 63 SCA3, median Scale for the Assessment and Rating of Ataxia (SARA) score = 5, 42% preataxic, and 14 gene‐negative controls) was scanned at 3T up ...
Thiago J. R. Rezende   +26 more
wiley   +1 more source

Intergenerational Succession on Family Farms: Evidence from Survey Data [PDF]

open access: yes
This study examines family farms and characteristics affecting farm succession. Based on a farm survey, three aspects of succession are analysed in the paper: the probability of family succession; the likelihood of having a successor designated; and the ...
Weiss, Christoph R.   +2 more
core   +4 more sources

EXPLICAŢII TERMINOLOGICE ALE CONCEPTULUI DREPTULUI LA MOŞTENIRE

open access: yesStudia Universitatis Moldaviae: Stiinte Sociale, 2009
The research of a law institution implies a detailed interpretation of the legal instruments specific for this field. The legal terms as inheritance, heir, deceased, inheritance part, succession represents basic pillars of right to inheritance.
USM ADMIN
doaj  

Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Long‐read sequencing and optical genome mapping technologies have the ability to detect large and complex structural variants. This has led to the discovery of novel pathogenic variants in neurodegenerative movement disorders. Thus, we aimed to systematically compare the SV detection capabilities of OGM and ONT in Parkinson's disease.
André Fienemann   +17 more
wiley   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina   +11 more
wiley   +1 more source

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