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  1. 21
    por Uller, Wibke, Alomari, Ahmad I.
    Publicado 2014
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    Portomesenteric thrombosis and hypertension in Klippel–Trenaunay syndrome
  2. 22
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    Klippel-Feil Syndrome and Unilateral Diaphragmatic Paralysis
  3. 23
    por Rush, Jeffrey S.
    Publicado 2016
    “…This review focuses on the flippases that participate in protein glycosylation in the ER.…”
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    Role of Flippases in Protein Glycosylation in the Endoplasmic Reticulum
  4. 24
    “…The aim of this study is to report the results of intensive therapy of lymphedema associated with Klippel-Trenaunay syndrome. A 24-year-old female patient reported that her family had observed edema in her right leg and port wine stains from birth. …”
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    Lymphedema in Klippel-Trenaunay Syndrome: Is It Possible to Normalize?
  5. 25
    “…We describe a patient with obstructive azoospermia and Klippel–Feil anomaly.…”
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    Azoospermia in a Male with Klippel–Feil Anomaly
  6. 26
    por Reyes, Fabian, Ma, Shugen
    Publicado 2017
    “…Metrics are derived to study the motion of the object and robot, showing that the addition of passive wheels to the snake robot helps to minimize slippage. However, the passive wheels do not have a significant impact on the force exerted onto the object. …”
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    Studying slippage on pushing applications with snake robots
  7. 27
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    Lymphangioma Circumscriptum in Vulva with Klippel-Trenaunay Syndrome
  8. 28
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    Klippel-Feil syndrom: a duplicated thumb
  9. 29
    por Onoda, Satoshi, Komagoe, Sho
    Publicado 2019
    “…INTRODUCTION: Since we performed lymphaticovenular anastomosis (LVA) for Klippel-Trenaunay-Weber syndrome and obtained relatively good results, we report the adaptation, effect of treatment, and mechanism of LVA. …”
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    Lymphaticovenular anastomosis for Klippel-Trenaunay-Weber syndrome
  10. 30
    “…PURPOSE: Klippel-Trenaunay syndrome (KTS) is a rare combined vascular malformation composed of capillary malformation, lymphatic and/or venous malformation and limb overgrowth, which commonly affects the extremities. …”
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    Orthopaedic diagnoses in patients with Klippel-Trenaunay syndrome
  11. 31
    “…Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterised by cutaneous capillary malformations, soft tissue and bone hypertrophy and venous varicosities. …”
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    Craniotomy in Klippel-Trenaunay syndrome: Concerns and challenges
  12. 32
    por Kim, El
    Publicado 2022
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    The Shunt Slippage: A Complication of Pumping Test
  13. 33
    “…BACKGROUND: The purpose of this study was to develop and validate reliable computed tomography (CT) imaging criteria for the diagnosis of gastric band slippage. MATERIAL AND METHODS: We retrospectively evaluated 67 patients for gastric band slippage using CT. …”
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    Computed Tomography Assessment of Gastric Band Slippage
  14. 34
    “…The Klippel-Trénaunay syndrome (KTS) is a rare form of a birth disorder that includes capillary malformation, hypertrophy of bones and soft tissues, and tortuous varicosities, as well as hypertrophy of the capillaries resulting in hemangiomas and port wine discoloration. …”
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    A Rare Case of Klippel-Trénaunay Syndrome
  15. 35
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    Complex Analysis: In the Spirit of Lipman Bers
  16. 36
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    Complex analysis: in the spirit of lipman bers
  17. 37
    “…The book is part biography and part collection of mathematical essays that gives the reader a perspective on the evolution of an interesting mathematical life. It is all about Lipman Bers, a giant in the mathematical world who lived in turbulent and exciting times. …”
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    Lipman Bers, a life in mathematics
  18. 38
    “…Designated proteins — flippases and scramblases — mediate this lipid movement between the bilayers. …”
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    Regulation of phospholipid distribution in the lipid bilayer by flippases and scramblases
  19. 39
    “…Here, we show that Drs2p, a type IV P-type ATPase required for phospholipid translocase (flippase) activity and transport vesicle budding from the TGN4–8, is an effector of PtdIns[4]P. …”
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    Regulation of a Golgi Flippase by Phosphoinositides and an ArfGEF
  20. 40
    “…Sturge–Weber syndrome in combination with Klippel–Trenaunay syndrome is unusual. Because of the rarity, we report here a 3-year-old boy who presented with overlapping features of both the syndromes.…”
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    OVERLAP OF STURGE–WEBER SYNDROME AND KLIPPEL–TRENAUNAY SYNDROME
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