LEADER 00785nam0-22002891i-450- 001 990001184110403321 035 $a000118411 035 $aFED01000118411 035 $a(Aleph)000118411FED01 035 $a000118411 100 $a20000920d1963----km-y0itay50------ba 101 1$aeng 200 1 $aStellar Interiors$fby MENZEL AND BHATNAGAR 210 $aLondon$cChapman & Hall$d1963 225 1 $a<>International Astrophysics Series 300 $aVI VOL. 700 1$aMenzel,$bDonald H.$012891 702 1$aBhatnagar,$bPrabhu Lal 702 1$aSen,$bHari K. 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990001184110403321 952 $a204-C-32$b1339$fMA1 959 $aMA1 996 $aStellar Interiors$9342348 997 $aUNINA DB $aING01 LEADER 02061nam 2200481 450 001 9910814031003321 005 20230807194000.0 010 $a1-4438-8469-3 035 $a(CKB)3710000000498447 035 $a(EBL)4534938 035 $a(MiAaPQ)EBC4534938 035 $a(Au-PeEL)EBL4534938 035 $a(CaPaEBR)ebr11215949 035 $a(CaONFJC)MIL845798 035 $a(OCoLC)927160075 035 $a(EXLCZ)993710000000498447 100 $a20160620h20152015 uy 0 101 0 $aeng 135 $aurcnu|||||||| 181 $2rdacontent 182 $2rdamedia 183 $2rdacarrier 200 12$aA colourful presence $ethe evolution of women's representation in Iranian cinema /$fby Maryam Ghorbankarimi 210 1$aNewcastle upon Tyne, England :$cCambridge Scholars Publishing,$d2015. 210 4$dİ2015 215 $a1 online resource (221 p.) 300 $aDescription based upon print version of record. 311 $a1-4438-8272-0 320 $aIncludes bibliographical references and filmographies. 330 $aThis book analyzes the changes in the representation of women in Iranian cinema since the 1960's, and investigates the reasons and motives for this. Iranian cinema, both before and after the Islamic Revolution, has been closely monitored by the ruling power, and has been utilized to relay messages and information that comply with the ruling ideology.However, it was only after the 1979 Revolution and the subsequent legitimization of cinema by the Islamic rule that cinema became widely accessible to the general public. Within this context, this book explores the changing roles of women in film pr 606 $aWomen in motion pictures 606 $aMotion pictures$zIran 615 0$aWomen in motion pictures. 615 0$aMotion pictures 676 $a791.43652042 700 $aGhorbankarimi$b Maryam$01647520 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910814031003321 996 $aA colourful presence$93995122 997 $aUNINA LEADER 04929nam 2200637 a 450 001 9910962560403321 005 20240416183152.0 010 $a9781898683834 010 $a1898683832 035 $a(CKB)2550000000084777 035 $a(EBL)1667668 035 $a(SSID)ssj0000598542 035 $a(PQKBManifestationID)12270778 035 $a(PQKBTitleCode)TC0000598542 035 $a(PQKBWorkID)10592008 035 $a(PQKB)11539475 035 $a(MiAaPQ)EBC3329142 035 $a(Au-PeEL)EBL3329142 035 $a(CaPaEBR)ebr10313242 035 $a(OCoLC)929120182 035 $a(Perlego)1974864 035 $a(EXLCZ)992550000000084777 100 $a20130815d2008 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aAngelman syndrome /$fBernard Dan 205 $a1st ed. 210 $aLondon $cMac Keith Press$d2008 215 $a1 online resource (192 p.) 225 0$aClinics in developmental medicine ;$vno. 177 300 $aDescription based upon print version of record. 311 08$a9781898683551 311 08$a1898683557 320 $aIncludes bibliographical references and index. 327 $aCONTENTS; AUTHORS' APPOINTMENTS; FOREWORD; 1 DR ANGELMAN'S SYNDROME Bernard Dan; Original report of Angelman syndrome; Dr Harry Angelman (Fig. 1.2); From puppet children to Angelman syndrome; Illustrations and derivations; From patient descriptions to diagnostic criteria; Angelman syndrome as a model; Conclusion; 2 NATURAL HISTORY Karine Pelc and Bernard Dan; Antenatal and perinatal period; Neonatal period; Infancy; Childhood; Adolescence; Adulthood; Conclusion; 3 A PERSONAL ACCOUNT Patrick Haverbeke; How an angel changed our life; Early problems with integration 327 $aOptions for Henri's educationThe road to diagnosis; Tools for communication; The difficult choice: putting Henri in a residential institution; Reorganising our family life; Time is passing: Henri becomes an adult; Henri, ambassador across the world; 4 MEDICAL GENETICS Bernard Dan; Chromosome 15q11-q13 deletion; Uniparental disomy; UBE3A mutation; Imprinting defect; Chromosomal aberration; Other identified genetic abnormalities; Genetic testing; Genetic counselling; Prenatal diagnosis; Risks associated with in vitro fertilisation; Conclusion; 5 MOLECULAR BIOLOGY Bernard Dan; Genomic imprinting 327 $aGenomic imprintingUBE3A gene expression; Ubiquitination; UBE3A gene expression; Ubiquitination; An integrative hypothesis; An integrative hypothesis; Possible targets for management; Possible targets for management; Conclusion; Conclusion; 6 DIFFERENTIAL DIAGNOSIS Bernard Dan; Cerebral palsy; Autistic spectrum; Lennox-Gastaut syndrome; Rett syndrome; Untreated phenylketonuria; Methylenetetrahydrofolate reductase deficiency; ATR-X syndrome; Gurrieri syndrome; Mowat-Wilson syndrome; Chromosomal abnormalities; Mosaic imprinting defects of 15q11-q13; Prader-Willi syndrome 327 $aInverted duplication of chromosome 15Conclusion; 7 BEHAVIOUR Bernard Dan; Happy disposition; Hyperactivity and impulsivity; Stereotypic behaviours; Autistic features; Social interaction; Behavioural adaptability; Interest profile; Oral behaviours; Conclusion; 8 PERCEPTION AND COGNITION Bernard Dan; Visual perception; Auditory and language perception; Somatosensory perception; Pain; Other perceptual modalities; Attention; 'Mental age'; Memory; Emotion; Conclusion; 9 COMMUNICATION Bernard Dan; General context of communication; Receptive verbal language; Expressive verbal language 327 $aExpressive non-verbal languageConclusion; 10 MOVEMENT AND POSTURAL CONTROL Bernard Dan and Guy Cheron; Alternative vs immature motor development; Early motor development; Later motor development; Motor signs; Balance; Oromotor function; Hand function; Walking; Other movements; Tremor vs myoclonus; Pathophysiology; Physical management; Pharmacological management; Conclusion; 11 EPILEPSY Bernard Dan and Stewart G. Boyd; Natural history of the seizure disorder; Seizure types; Epileptic syndrome; Convulsive status epilepticus; Non-convulsive status epilepticus; Management; Conclusion 327 $a12 SLEEP Bernard Dan and Stewart G. Boyd 330 $a A comprehensive review of clinical and genetic issues, natural history, possible pathophysiological pathways, specific clinical problems (motor impairment, behaviour, learning difficulties, communication, sleep, epilepsy), clinical neurophysiology, neuropathology, rehabilitation and basic research in the field of Angelman syndrome. 410 0$a1st 606 $aAngelman syndrome 615 0$aAngelman syndrome. 676 $a616.853 700 $aDan$b Bernard$01813695 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910962560403321 996 $aAngelman syndrome$94367078 997 $aUNINA