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Mostrando 101 - 120 Resultados de 2,550 Para Buscar 'Klippan~', tiempo de consulta: 3.42s Limitar resultados
  1. 101
    por Feinsod, Moshe
    Publicado 2012
    “…Lipman Halpern was born in 1902 into a family of Grand Rabbis who lived in Bialystok from the mid-nineteenth century. …”
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    The Neurologist Lipman Halpern—Author of the Oath of the Hebrew Physician
  2. 102
    “…MATERIALS AND METHODS: Our study has included a total number of 150 inmates, of both genders, from Lipjan prison house in Kosovo. RESULTS: Oral health condition of inmates in Lipjan prison house is severe; the average value of DMFT is 8.44: for minors 6.22, while for adults 9.55. …”
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    Oral Health of Lipjan Convicts: Kosovo Prison House
  3. 103
    por Ho, Anh-Van, Hirai, Shinichi
    Publicado 2014
    “…Although this phenomenon is dominant for a very short time prior to gross slippage, localized slippage is a crucial factor for any to-be-developed soft sensing system to respond to slippage before it occurs. …”
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    Mechanics of localized slippage in tactile sensing: and application to soft sensing systems
  4. 104
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    Klippel Trenaunay Syndrome-The Pulsating Calf; A Rare Case Presentation
  5. 105
    “…Klippel–Trenaunay syndrome is an uncommon, infrequent, congenital disorder characterized by a triad of capillary malformation, varicosities, and tissue and bone hypertrophy. …”
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    Klippel–Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review
  6. 106
    “…CONTEXT: Klippel–Trenaunay–Weber syndrome (KTWS) is a rare disease characterized by a triad of venous malformations, vascular skin nevus and asymmetric hypertrophy of bone and soft tissue. …”
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    Fetal Klippel–Trenaunay–Weber Syndrome: Antenatal Diagnosis and Postnatal Management
  7. 107
    por Chi, Lai Man, Lam, Sik Lok
    Publicado 2005
    “…The results of this study confirm the hairpin loop structures and explain how slippage occurs during DNA replication.…”
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    Structural roles of CTG repeats in slippage expansion during DNA replication
  8. 108
    “…From these data, we conclude that caspase activity is not required for a functional MC or for mitotic slippage.…”
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    Caspase activity is not required for the mitotic checkpoint or mitotic slippage in human cells
  9. 109
    “…BACKGROUND: Klippel-Trenaunay-Weber Syndrome (KTWS) is a rare neurocutaneous syndrome. …”
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    Klippel-Trenaunay-Weber Syndrome with Hemimegalencephaly; Report of a Pediatric Case
  10. 110
    “…BACKGROUND: Uncommonly, Klippel–Feil syndrome (KFS) has been associated with intracranial or spinal tumors, most frequently dermoid or epidermoid cysts. …”
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    Klippel–Feil syndrome associated with a craniocervico-thoracic dermoid cyst
  11. 111
    “…Limiting graft slippage will reduce associated complications. We sought to compare the in vitro mechanical properties and in vivo joint stabilization, postoperative limb use, and graft incorporation of the novel GraftGrab™ (GG) device designed to reduce hamstring graft tibial fixation slippage with the commercially available bioabsorbable Bio-Post™ and spiked washer (BP). …”
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    Novel anterior cruciate ligament graft fixation device reduces slippage
  12. 112
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    Pore Structure and Limit Pressure of Gas Slippage Effect in Tight Sandstone
  13. 113
    “…Klippel-Trénaunay syndrome (KTS) is a rare vascular congenital anomaly affecting less than 200,000 people in the United States. …”
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    Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation
  14. 114
    “…Our results suggest that an unknown mechanism, possibly a protein with flippase-like activity, acts in conjunction with known flippases to regulate PS translocation.…”
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    Asymmetric distribution of phosphatidylserine is generated in the absence of phospholipid flippases in Saccharomyces cerevisiae
  15. 115
    “…Four types and two subtypes have been described where subtype ‘a’ present only with cutaneous form and subtype ‘b’ also with systemic association like in Sturge-Weber syndrome or Klippel-Trenaunay syndrome. Hereby, we report a case where our patient presented with port-wine stain, Nevus of Ota, Sturge-Weber syndrome, and Klippel-Trenaunay syndrome; which has made it a rare combination.…”
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    Phakomatosis Pigmentovascularis Presenting with Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome
  16. 116
    “…Flippases function in the formation of transport vesicles, but the mechanism remains unknown. …”
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    Inositol Depletion Restores Vesicle Transport in Yeast Phospholipid Flippase Mutants
  17. 117
    “…INTRODUCTION: Klippel-Trenaunay-Weber syndrome (KTWS) is a rare syndrome in which patients usually present with cutaneous hemangiomas, venous varicosities, and bone and soft tissue hypertrophy of the affected limb. …”
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    Glioblastoma multiforme in Klippel-Trenaunay-Weber syndrome: a case report
  18. 118
    “…Klippel-Trenaunay syndrome (KTS) is a rare complex malformation characterized by the clinical triad of capillary malformations, soft tissue and bone hypertrophy, and venous/lymphatic malformation. …”
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    Management of Femoral Shaft Fracture in Klippel-Trenaunay Syndrome with External Fixator
  19. 119
    “…We suggest that markers of mitotic slippage be assessed in future studies of senescence to determine the extent of mitotic slippage in the induction of cellular senescence.…”
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    PKCι depletion initiates mitotic slippage-induced senescence in glioblastoma
  20. 120
    “…AIM: This is to report a case of Klippel Trenauay Weber syndrome in a fifteen year old Nigerian boy. …”
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    Klippel Trenaunay Syndrome: A Case Report in an Adolescent Nigerian Boy
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