1,723,259 research outputs found
Letter from Mrs. Robert D. Loken, December 3, 1967
No full textLetter from Mrs. Robert D. Loken to Fayez Sayegh, December 3, 1967, regarding his appearance on the David Susskind show and the Arab-Israeli conflict; includes copy of a letter sent to David Susskind on the same topic
Replication Data for: "Infant Health Care and Long-Term Outcomes"
No full textBütikofer, Aline, Loken, Katrine, and Salvanes, Kjell, (2019) "Infant Health Care and Long-Term Outcomes." Review of Economics and Statistics 101:2, 341-354
Replication Data for: "Infant Health Care and Long-Term Outcomes"
No full textBütikofer, Aline, Loken, Katrine, and Salvanes, Kjell, (2019) "Infant Health Care and Long-Term Outcomes." Review of Economics and Statistics 101:2, 341-354
Senior-Loken syndrome in an Iranian family
No full textSenior-Loken syndrome is a rare entity that combines familial juvenile nephro-nophthisis with retinal dystrophy. Herein, we report Senior-Loken syndrome in six members of an Iranian family with progressive blindness and renal failure since childhood. Although, this syn-drome was reported from other parts of the world, report of six members of one family with this syndrome is rare. To the best of our knowledge, this is the first report from Iran
Robert D. Loken, Manpower development in Africa
No full textD'Hauteville Béatrix. Robert D. Loken, Manpower development in Africa. In: Tiers-Monde, tome 11, n°44, 1970. La ville et l'organisation de l'espace dans les pays en voie de développement. pp. 892-893
Senior-Loken Syndrome in a Saudi Child
No full textSenior-Loken syndrome is a rare syndrome of retinopathy and nephrono-phthisis. The clinical features of this syndrome include renal involvement, ocular involve-ment, retinitis pigmentosa and other systemic involvement. We describe an 11-year-old Saudi girl who was diagnosed to have this syndrome. To the best of our knowledge, this is the first report of this syndrome from the Arabian Peninsula
Design Strategy for Tourism Object Management Case Study at Loken Barn Resort Karo District, North Sumatra Province
No full textKaro Regency is an area that has so many natural attractions. Loken Barn Resort at Pengambatan, Gajah Bobok Street, Merek District, Karo Regency, North Sumatra Province 22173, which is managed and developed by an owner of Loken Barn Resort. The purpose of this study is to analyze the owner's strategy in managing and developing the Loken Barn Resort location in Karo Regency. This type of research is descriptive qualitative research. Sources of research materials are key information and related information in this study. Data collection techniques in this study were observation, interview documentation, and literature study. Data analysis techniques used with data collection, data simplification, data presentation, and conclusions. The results of this study indicate that in managing and developing tourist destinations it is considered that it is still not optimal in the management and development of Loken Barn Resort attractions due to limited professional staff and human resources and the lack of budget to manage and develop Loken Barn Resort attractions
Senior Loken Syndrome
No full textThe etiology of ESRD under the age of 20 almost is the inherited kidney disease or congenital disorders of urinary tract. NPHP/ medullary cystic disease includes a group of tubulo- genetic kidney disorders. NPHP is the cause of 15-20% ESRD in children and adolescents. The extra renal manifestations include: oculomotor Apraxia(Cogan syndrome), mental retardation, retinitis pigmentosa, (Senior- Loken syndrome) liver fibrosis and skeletal disorders. Recently, on the basis of genetics and type of the protein product of these mutations, NPHP is divided to 6 types. The presented case is a 17 year old boy with end stage renal disease that he has been managed with hemodialysis. As the patient has polyuria and disturbance in vision from childhood and on physical examination he had retinitis pigmentosa and horizontal nystagmus with a history of chronic kidney disease in his 12 years old sister, and familial marriage between his parents, we suggest NPHP4 for the patient
Genetic testing for Senior-Loken syndrome
No full textAbstract
We studied the scientific literature and disease guidelines in order to summarize the clinical utility of genetic testing for Senior- Loken syndrome (SLSN). SLSN is inherited in an autosomal recessive manner, has a prevalence of one in a million, and is caused by variations in CEP164, CEP290, INVS, IQCB1, NPHP1, NPHP3, NPHP4, SDCCAG8, TRAF3IP1 and WDR19 genes. Clinical diagnosis is based on kidney (urine analysis, abdominal ultrasound, kidney function) and eye assessment (visual acuity test, fundus examination, refraction defects, color testing and electroretinography). The genetic test is useful for confirming diagnosis, and for differential diagnosis, couple risk assessment and access to clinical trials.</jats:p
Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness
No full textTwo siblings with Senior-Loken syndrome are described. The need for a full evaluation of renal function and hearing in children with a retinal dystrophy is emphasised
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