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  1. 61
    “…Klippel–Trenaunay syndrome is characterized by a combination of vascular abnormalities and limb hypertrophy. …”
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    Pleural effusion in Klippel–Trenaunay syndrome: an uncommon manifestation
  2. 62
    “…Here, we present a Li(+)-centered G-quadruplex (LiGQ) as a class of single-ion conductor based on directional Li(+) slippage at the microscopic level. A guanine derivative with liquid crystalline moieties is self-assembled to form a hexagonal ordered columnar structure in the LiGQ, thereby yielding one-dimensional central channels that provide weak ion-dipole interaction and straightforward ionic pathways. …”
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    Ion slippage through Li(+)-centered G-quadruplex
  3. 63
    por Gerigk, Frank
    Publicado 2001
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    The effect of phase slippage in multicell cavities on longitudinal beam dynamics
  4. 64
    por Gerigk, F
    Publicado 2001
    “…Using multicell cavities at velocitiesdifferent from their design value yields phase slippage in the single cells, thereby reducing energy gain and longitudinal focusing. …”
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    The Effect of Phase Slippage in Multicell Cavities on Longitudinal Beam Dynamics
  5. 65
    “…Cervical spine assessment is an important step in patients who sustained trauma. Klippel-Feil syndrome (KFS) is a complex syndrome with an abnormal fusion of cervical vertebrae at C2 and C3, which is caused by a failure in the division or normal segmentation of the cervical spine vertebrae in early fetal development. …”
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    A Case Report of Klippel-Feil Syndrome Presenting as Tetraplegia
  6. 66
    “…First described by the French physicians Marcel Klippel and Paul Trenaunay, in 1900, KTWS has a clinically incidence of 2–5/100000. …”
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    Klippel-Trenaunay-Weber syndrome: Oro-dental manifestations and management
  7. 67
    “…Klippel-Trénaunay syndrome is typically a complex combined capillary-lymphatic-venous malformation in lower limb. …”
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    Gastrointestinal involvement in Klippel-Trénaunay syndrome: pathophysiology, evaluation, and management
  8. 68
    “…Klippel–Trenaunay syndrome and Sturge–Weber syndrome are rare disorders with neurologic and cutaneous signs of vascular origin. …”
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    Klippel–Trenaunay and Sturge–Weber overlap syndrome with phakomatosis pigmentovascularis
  9. 69
    “…However unwinding traces showed a remarkable sawtooth pattern where processive unwinding was repeatedly interrupted by sudden slippage events, ultimately preventing unwinding over a substantial distance. …”
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    ATP-Induced Helicase Slippage Reveals Highly Coordinated Subunits
  10. 70
    “…A diagnosis of Phacomatosis cesioflammea or Phacomatosis pigmentovasularis Type II with Klippel Trenaunay syndrome was made. The case is being reported on account of its rarity.…”
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    Phacomatosis cesioflammea with Klippel Trenaunay syndrome: A rare association
  11. 71
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    A Sporadic Case of Klippel-Feil Syndrome Type 2
  12. 72
    “…Klippel Trenaunay syndrome (KTS) is a rare congenital disease characterized by a triad of cutaneous hemangioma, varicose veins and bone or soft tissue hypertrophy. …”
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    Successful management of pregnancy in an African woman with Klippel Trenaunay syndrome
  13. 73
    “…We present a case with Klippel-Trenaunay (KT) syndrome that had unilateral mature cataract and vitreoretinopathy. …”
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    Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome
  14. 74
    “…Klippel–Trenaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, atypical venous malformations and varicosities and bony and/or soft tissue hypertrophy. …”
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    Ethanol sclerotherapy of rectal venous abnormalities in Klippel–Trenaunay syndrome
  15. 75
    “…We have screened through 201 enhancer-trap flippase lines to identify lines that produce useful clone patterns in the adult ovary. …”
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    Enhancer-Trap Flippase Lines for Clonal Analysis in the Drosophila Ovary
  16. 76
    “…Klippel–Trénaunay syndrome (KTS or KT) is an infrequently seen dermatological syndrome, which is often viewed as a triad of vascular malformation (capillary malformations or port-wine brands), venous varicosity, and soft tissue and/or bony hypertrophy. …”
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    Klippel–Trénaunay Syndrome – A Very Rare and Interesting Syndrome
  17. 77
    por Alaqeel, Aqeel Abdullah
    Publicado 2014
    “…Klippel-Feil syndrome is defined as the fusion of cervical vertebra with associated congenital anomalies but was rarely reported to be associated with Mondini Malformation. …”
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    Severe Klippel-Feil syndrome with Mondini malformation of inner ear
  18. 78
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    A rare paediatric case of Klippel-Trenaunay-Weber syndrome
  19. 79
    “…The slippage efficiency is ∼2% in Turnip mosaic virus and slippage is inhibited by mutations in the GAAAAAA sequence. …”
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    Transcriptional slippage in the positive-sense RNA virus family Potyviridae
  20. 80
    “…We suggest that Mcl-1 competes with Cyclin B1 for binding to components of the proteolysis machinery, thereby slowing down the slow degradation of Cyclin B1 responsible for slippage. Thus, modulating Mcl-1 dynamics influences both death-in-mitosis and slippage. …”
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    Mcl-1 dynamics influence mitotic slippage and death in mitosis
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