GEORGIANS IN SAFAVID IRAN: ABOUT SOME PERSIAN AND ARABIC INSCRIPTIONS OF THE SEVENTEENTH CENTURY RELATED TO THE REPRESETATIVES OF THE UNDILADZE FAMILY

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The paper discusses a number of Persian and Arabic inscriptions related to Allahverdi Khan (d. 1613) and his eldest son and successor Imamquli Khan (d. 1632), the most famous and influential representatives of the Undiladze family of Georgian gholams, who occupied key positions and played an important role in the military-political and administrative arena of Safavid Iran during the reign of Shah ‘Abbas I (r. 1587-1629). Reference is, in particular, to the following epigraphic materials from the first quarter of the seventeenth century: Arabic and Persian inscriptions (dated 1021 and 1022 AH) from the domed mausoleum of Allahverdi Khan in Mashhad; Arabic inscription (dated 1031 AH) on the north exterior entrance portal of the Jame‘-e ‘Atiq Mosque of Shiraz; Persian and Arabic inscriptions (dated 1032 and 1033 AH) from the Imamzadegan-e Hefdah-Tan in Golpayegan; Persian inscriptions on Portuguese cannons taken as spoils of war by the Iranians under the command of Imamquli Khan during the capture of Hormuz in 1622. These inscriptions provide quite valuable additional material for the study of various aspects of the history of the Undiladze family. The authors are most grateful to Prof. Naufomi Abe (University of Tokyo, Japan), Prof Jose Francisco Cutillas Ferrer (University of Alicante, Spain), Prof. May Farhat (Holy Spirit University of Kaslik, Lebanon), and Dr. Maka Natadze (Embassy of Georgia in the Islamic Republic of Iran), for their generous help with some of the references.

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  • THE COUNTRIES AND PEOPLES OF THE NEAR AND MIDDLE EAST
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Iran under the Safavids
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List of illustrations Map Acknowledgements 1. The Lords of Ardabil 2. Theocratic state: the reign of Shah Isma'il I (1501-1524) 3. Internal dissensions and external foes: the Safavid state from 1524 to 1588 4. The Safavid empire at the height of its power under Shah 'Abbas the Great (1588-1629) 5. Relations with the West during the Safavid period 6. The flowering of the arts under the Safavids 7. 'Isfahan is half the world' - Shah 'Abbas's Isfahan 8. The social and economic structure of the Safavid state 9. Intellectual life under the Safavids 10. Decline and fall of the Safavids Notes Index.

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Village parents in Pyrenean and Alpine districts (Bourdieu 1962, 1976; Cole and Wolf 1974; Collomp 1984; Douglass I975), Germany (Berkner 1977; Golde I975), large parts of Western Ireland (Arensberg 1968; Scheper-Hughes 1979), and other regions (Berkner 1972; Hansen I977; Lison 1974, 1977; O'Neill 1983; Vernier 1984) commonly assign their children unequal rights, duties, and legacies with reference cultural norms that define ideal characteristics of major and minor heirs. Individual offspring typically function outside their families in accordance with their places in these domestic orders of precedence. Their differential public behavior furthers development of distinct status groups at community level. This sorting of offspring into distinct family roles and status groups is an ongoing process subject changing interests, claims, and capabilities of property owners and their expected heirs (see Medick and Sabean 1984: 16). Customary practice may initially motivate parents designate eldest son as their expected major heir (e.g., Bourdieu 1962; Collomp 1984; Lison 1974), but they usually retain right replace this child at a later date with a more promising successor. In most preferential inheritance societies, Ethnohistory 34:2 (Spring 1987). Copyright ? by American Society for Ethnohistory. ccc ooi4-I8oi/87/$I.50. This content downloaded from 207.46.13.16 on Thu, 16 Jun 2016 06:17:25 UTC All use subject http://about.jstor.org/terms 172 Rainer Lutz Bauer parents aim their strategies for transmitting their estates at improving social positions of their families (e.g., Bourdieu 1976: izz; Lison 1974: 74; Vernier 1984: 40). They tend encourage all their children compete for larger portions of their estates and hope for individual advancement on basis of their relative contributions realization of this aim (see ScheperHughes 1979: 163-85). This underscores equivocal statuses of individual heirs-to-be and uncertain paths of specific family histories. A key issue underlying negotiation of differential heirship statuses is relative power of actors bargaining over transmission of an estate. Among nineteenth-century European peasants, ownership of land was premier source of power. This reinforced domination of parents over children, major heirs over minor heirs, and largeholders over smallholders. However, villagers with subordinate statuses might strive improve their life options by exploiting resources outside purview of local power holders. They sometimes prospered in this endeavor as a result of exceptional abilities or exceptional circumstance. Witness successful transatlantic migrants (indianos) of nineteenth-century Northern Spain (Ferrer del Rio I85I: i6zo; Kasdan 1965; Kenny 1976). Those who returned Spain and settled in their natal communities were often able negotiate new heirship or family statuses with unexpected strength. As a result, social differentiation produced by inheritance processes acted back upon domestic relations. In following pages, I analyze relationship between inheritance practices and inequality in a local context. I describe family and inheritance systems of villagers of Sierra del Caurel, an agropastoral district in Spanish province of Lugo, as coiistituted in century prior Spanish Civil War. This period is characterized by relatively stable patterns of behavior that formed in early decades of nineteenth century and changed substantially after war. My description focuses on socialization process whereby members of an offspring set are distinguished as individuals and social actors by their recognized claims major and minor shares of their parents' estate. I show how these claims are negotiated by parents and their children with reference interacting norms that emphasize precedence of eldest sons, required competencies of major and minor heirs, and integrity of patrimonies. My aim is reveal how inequality develops within particular families, is extended and reinforced at community level, and is transmitted between generations. The Inheritance System Property and family in Sierra del Caurel are bound together in a complex conceptualized by Caurelaos-the inhabitants of sierra-in notion of casa (house) (see Lis6n I974, I977). The casa centers on an agropastoral estate composed of real property and connected rights in communal doThis content downloaded from 207.46.13.16 on Thu, 16 Jun 2016 06:17:25 UTC All use subject http://about.jstor.org/terms Inheritance in a Spanish Community main. Preferential inheritance practices tend perpetuate a link between this estate and a particular family line. This link is essence of casa. Cultural norms favor a single child in each generation of a family as major heir of casa. This child receives (improvement) from each of his parents. The typically comprises the third and fifth (el tercio y quinto) or (after establishment of Spanish Civil Code in 1889) two-thirds of parents' estate. All children in a family, including major heir, share equally in their parents' residual estate. Consequently, even in a large offspring set, a millorado (improved heir) inherits bulk of his house's patrimony. This customary division of property sharply differentiates life chances of major and minor heirs within a given family. The enables major heir become a fully enfranchised community member: it ideally gives him a complete and viable farmstead, right and obligation to marry in his natal house (casarse en casa), and right and duty speak for his casa. The legitimas (legally required minimal inheritance shares) of minor heirs secure their place in Caurel's domestic economy and simultaneously restrict their claims on community and casa. Legitimas ideally serve capitalize minor heirs' marriages with major heirs of other casas, support their independent farming or business ventures, or otherwise provide them livelihoods of their own. In practice, minor heirs often remain lifelong dependents of their natal casas-as celibate residents, seasonal migrant laborers, or operators of exiguous farms supported by their favored sibling. Cultural preferences identify ideal major heir of a casa. Lis6n describes Caurel and adjacent mountain districts of eastern Lugo province as portion of region of Galicia in which patrilineal and patrilocal millora is most deeply embedded (I977: I75). He goes on say that in principle tends marry an eldest son en casa, whether or not he is first offspring, or at least a son of any kind; in case there are no [sons], it is a daughter, preferably eldest, who receives manda (i.e., millora) (1977: I75). To what extent are these cultural preferences realized in practice? Consider sex and birth rank of individuals who were married en casa in parish of San Juan de Seoane in I940. I identified a total of 48 such apparent major heirs (or heirs-to-be) in Caurel's Padr6n Municipal, township's household register (Ayuntamiento I940). All of these individuals had at least one surviving sibling; all but six had two or more. Twenty-seven (56 percent) were eldest sons. Sixteen of zz who remained were daughters. It is significant that half of these favored daughters were eldest children. The order of preference for major heirs suggested by 1940 Padr6n approximates Lis6n's observation. Despite myriad factors that tend constrain agreement between cultural norms and practice-among them, absence of male offspring, incapacity or disinclination of eldest sons, conflicts between parents and their children-it is clear that eldest sons are I73 This content downloaded from 207.46.13.16 on Thu, 16 Jun 2016 06:17:25 UTC All use subject http://about.jstor.org/terms

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  • 10.3748/wjg.v18.i15.1840
Gastric angiodysplasia in a hereditary hemorrhagic telangiectasia type 2 patient
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  • World Journal of Gastroenterology
  • Minsu Ha

Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people. Clinical diagnosis of HHT is made when a person presents three of the following four criteria: family history, recurrent nosebleeds, mucocutaneous telangiectasis, and arteriovenous malformations (AVM) in the brain, lung, liver and gastrointestinal (GI) tract. Although epistaxis is the most common presenting symptom, AVMs affecting the lungs, brain and GI tract provoke a more serious outcome. Heterozygous mutations in endoglin, activin receptor-like kinase 1 (ACVRL1; ALK1), and SMAD4, the genes involved in the transforming growth factor-β family signaling cascade, cause HHT. We report here the case of a 63 year-old male patient who presented melena and GI bleeding episodes, proven to be caused by bleeding from multiple gastric angiodysplasia. Esophagogastroduodenoscopy revealed multiple angiodysplasia throughout the stomach. Endoscopic argon plasma coagulation was performed to control bleeding from a gastric angiodysplasia. The patient has been admitted several times with episodes of hemoptysis and hematochezia. One year ago, the patient was hospitalized due to right-sided weakness, which was caused by left basal ganglia hemorrhage as the part of HHT presentation. In family history, the patient's mother and elder sister had died, due to intracranial hemorrhage, and his eldest son has been suffered from recurrent epistaxis for 20 years. A genetic study revealed a mutation in exon 3 of ALK1 (c.199C > T; p.Arg67Trp) in the proband and his eldest son presenting epistaxis.

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  • Rupa Mehta + 2 more

<p>Branchial cleft anomalies comprise approximately 30% of congenital neck mass and present as cyst, sinus or fistula. They occur due to disturbance in the maturation of the branchial apparatus during fetal development. They are congenital lesions usually present in childhood, but they are usually diagnosed in later childhood or early adulthood because of enlargement or infection. Branchial cleft fistulae are usually diagnosed earlier than cysts. Correct diagnosis leads to proper management. Complete surgical excision is the treatment of choice. Second branchial cleft and pouch anomalies are commonest amongst all branchial cleft lesions, but complete second branchial cleft anomalies with external and internal opening is rare. Branchial anomalies with family history are also very rare. Here we present a case report of complete branchial fistula with family history which was managed by complete excision of fistula through transcervical and transoral approaches. 3 members of one family in 2 generations presented with branchial apparatus anomalies (father and his two children, elder son and younger daughter). All of them were having branchial fistula on right side of neck since birth.</p>

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  • Research Article
  • Cite Count Icon 31
  • 10.2471/blt.11.094474
The voice of the most vulnerable: lessons from the nuclear crisis in Fukushima, Japan
  • Apr 24, 2012
  • Bulletin of the World Health Organization
  • A Sugimoto + 4 more

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