Akibat Hukum terhadap Penghibahan Seluruh Harta Warisan oleh Pewaris Sehingga Melanggar Legitime Portie Ahli Waris Ditinjau dari Kuhperdata (Studi Putusan Nomor 188/pdt.g/2013/pn.smg) [PDF]
In any society, a hibah (grant) is not uncommon; it is done by a person as the realization of his freedom to organize his property. However, it is necessary to know that has its own rule which has to be obeyed.
WIJAYA, R. (RIVERA)
core
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 INSTITUTION OF RENUNCIATION OF INHERITANCE: HISTORY OF FORMATION AND DEVELOPMENT
Recently, the Russian legal doctrine has begun to pay more attention to the study of the legal nature of the refusal of inheritance, but most studies are devoted to the analysis of the current state of the institute, including the consideration of the ...
M. Bychko, I. Komarevtseva
doaj
KEDUDUKAN KELEBIHAN HARTA WARISAN (RADD) UNTUK JANDA DAN DUDA DALAM HUKUM WARIS ISLAM
This study aims to find out how current legal devices could give legal certainty on excess of family heritage partition (radd) for widowers and widows in Islamic laws as well as analyse judicial consideration on which matters regarding excess of family ...
Iwan Setyo Utomo
doaj +1 more source
Munasakhat; Metode Praktis Dalam Pembagian Harta Waris [PDF]
This study aims to find practical methods in the division of inheritance in a situation where one heir dies before the inheritance of first mayyit allocated, with one practical step, without counting the manual portion of each heir of first mayyit and ...
Barakah, A. (Ainun)
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Diagnostic Utility of the ATG9A Ratio in AP‐4–Associated Hereditary Spastic Paraplegia
ABSTRACT Adaptor protein complex 4–associated hereditary spastic paraplegia (AP‐4‐HSP), a childhood‐onset neurogenetic disorder and frequent mimic of cerebral palsy, is caused by biallelic variants in the adaptor protein complex 4 (AP‐4) subunit genes (AP4B1 [for SPG47], AP4M1 [for SPG50], AP4E1 [for SPG51], and AP4S1 [for SPG52]).
Habibah A. P. Agianda +12 more
wiley +1 more source
The Practice of Hibah as a Substitute Heir Among the Javanese Family [PDF]
This paper is an attempt to discuss the tradition of bequest or hibah as an inheritance, in which the wealth is distributed before the parents passed away among Javanese Family in Selesai Langkat. Data collection used qualitative method and phenomenology
Sukiati, S. (Sukiati)
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Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
wiley +1 more source
Surveying homicide as the real barriers of inheritance [PDF]
There are times when some of the heir qualities cause them to bedebarred from coming into their inheritance which are calledinheritance barriers. In spite of contradictions among the jurists ofIslamic faiths on the number of inheritance barriers, they ...
MORTEZA Tabib, Mohsen Akbari
doaj
Legal Complaint Against Dole [PDF]
This legal complaint was filed by the Conrad & Scherer law firm on April 28, 2009 in California state court in Los Angeles against the Dole Corporation.
Grunwald, David
core +1 more source

