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  1. 1281
    por Huegel, Ulrike, Baumgartner, Iris
    Publicado 2019
    “…Klippel-Trénaunay syndrome is characterized by a persistent lateral embryonic vein. …”
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    Implementation of new endovenous treatments in therapy for lateral embryonic veins
  2. 1282
    “…We report a case of Wildervanck syndrome exhibiting Klippel–Feil anomaly, Duane's retraction syndrome and congenital deafness. …”
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    Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation
  3. 1283
    por Goel, Atul
    Publicado 2018
    “…Assimilation of the atlas, C2–3 fusion, the Klippel-Feil abnormality, and pancervical fusion are amongst the more common types of bone abnormalities. …”
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    Cervical Fusion as a Protective Response to Craniovertebral Junction Instability: A Novel Concept
  4. 1284
    “…The complex malformations, such as, Klippel-Trenaunay Syndrome are much less commonly encountered lesions. …”
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    Clinical course of pediatric large vascular anomalies located in the extremities
  5. 1285
    “…In Klippel–Trenaunay syndrome, vascular malformations are not only in skin and superficial soft tissues but also in deep tissues like muscles bones and joints. …”
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    Total knee arthroplasty in vascular malformation
  6. 1286
    Publicado 1987
    Tabla de Contenidos: “…I believe in you / Frank Loesser (5:50) -- Love theme from "Spartacus" / Alex North (5:07) -- Granados /after the theme by Enrique Granados (5:51) -- My foolish heart / Victor Young, Ned Washington (4:47) --I loves you, Porgy / George Gershwin, DuBose Heyward, Ira Gershwin (5:50) -- How about you / Burton Lane, Arthur Freed (2:46) -- I've got you under my skin /Cole Porter (3:22) -- 'Round about midnight /Thelonious Monk, Cootie Williams, Bernie Hanighen (6:29) -- Elsa / Earl Zindars (4:20) -- A sleepin' bee / Harold Arlen, Truman Capote (5:54) -- Pavane / after a theme by Gabriel Fauré (3:57) -- Little Lulu /Buddy Kaye, Fred Wise, Sidney Lippman (3:52)…”
    CD Audiom
    Bill Evans
  7. 1287
    “…The differential diagnoses include anencephaly with spinal retroflexion, Klippel–Fiel syndrome, nuchal tumors such as teratoma, goiter, and lymphangioma and Jarcho–Levin syndrome. …”
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    Iniencephaly clausus: A case report with review of literature
  8. 1288
    “…Depending on their etiology, they can be categorized as congenital-including blue rubber bleb nevus syndrome, Klippel-Trenaunay syndrome, and hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)-or compressive-including "nutcracker" syndrome, median arcuate ligament syndrome, Cockett syndrome (also known as May-Thurner syndrome), and superior mesenteric artery syndrome. …”
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    Abdominal vascular syndromes: characteristic imaging findings
  9. 1289
    “…We here report a rare congenital AVM anomaly called Klippel-Trenaunay-Parks-Weber syndrome as a cause of massive hemoptysis and utility of double turn CT in diagnosing AVM as a cause of hemoptysis.…”
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    Hemoptysis: Beyond routine chest computed tomography and bronchoscopy
  10. 1290
    “…These include pentalogy of Cantrell, Klippel-Feil syndrome, cleidocranial dysplasia, Poland syndrome, osteopetrosis, neurofibromatosis type 1, Marfan syndrome, Gardner syndrome, systemic sclerosis, relapsing polychondritis, polymyositis/dermatomyositis, ankylosing spondylitis, hyperparathyroidism, rickets, sickle cell anemia, thalassemia, tuberculosis, septic arthritis of the sternoclavicular joint, elastofibroma dorsi, and sternal dehiscence.…”
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    Imaging of Thoracic Wall Abnormalities
  11. 1291
    “…Sprengel deformity is a congenital anomaly arising mainly in the shoulder girdle, associated with elevation of dysplastic scapula. skeletal anomalies, mainly Klippel-Feil syndrome, hemivertebrae, and omovertebral bone may be present along Sprengel anomaly. …”
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    Cervical myelopathy secondary to omovertebral bone in the pediatric patient with Sprengel deformity
  12. 1292
    “…Klippel-Feil syndrome (KFS) is characterized by failed segmentation of the cervical spine leading to inappropriately fused vertebral bodies. …”
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    Images in Spine: A Rare Abnormal Bony Fusion
  13. 1293
    “…Pediatric nonaortic arterial aneurysms are uncommon diagnoses and can be affiliated with underlying conditions, which include neurofibromatosis I, Ehlers-Danlos type IV syndrome, Kawasaki disease, Marfan syndrome, and Loeys-Dietz, polyarteritis nodosa, as well as Klippel-Trenauny syndrome. The standard of care has been early surgical excision and arterial reconstruction when indicated. …”
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    Recurrent brachial artery aneurysm repair in a child managed with Gore-Tex conduit reinforcement
  14. 1294
    “…We report the case of an 18-year-old woman who presented with primary amenorrhea, right kidney, Arnold-Chiari malformation, and Klippel-Feil syndrome. In addition, the patient showed the following unusual features: right ovarian and Skenes gland agenesis, cubitus valgus with hyperextension and decreased range of motion at elbows, and facial changes. …”
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    MURCS Association with Partial Duplication of the Distal Long Chromosome 5 and Unilateral Ovarian Agenesis
  15. 1295
    “…In the current review, four overgrowth syndromes were characterized (Proteus syndrome, Klippel-Trenaunay-Weber syndrome, Madelung's disease, and neurofibromatosis type I) and illustrated using cases from our institution. …”
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    Differential Diagnoses of Overgrowth Syndromes: The Most Important Clinical and Radiological Disease Manifestations
  16. 1296
    “…Sprengel shoulder is often associated with Klippel–Feil syndrome and other congenital skeletal deformities. …”
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    The Rare Sprengel Deformity: Our Experience with Three Cases
  17. 1297
    “…Anomalous marginal veins of the trunk or extremities are congenitally incompetent entities found in association with phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-related overgrowth syndromes, such as Klippel-Trénaunay syndrome and congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal deformities (CLOVES) syndrome. …”
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    Mechanochemical and surgical ablation of an anomalous upper extremity marginal vein in CLOVES syndrome identifies PIK3CA as the culprit gene mutation
  18. 1298
    “…BACKGROUND: PIK3CA-Related Overgrowth Spectrum (PROS) are rare syndromes caused by a mutation in the PIK3CA gene, including fibroadipose hyperplasia or overgrowth; congenital lipomatous overgrowth, vascular malformations, epidermal nevi, scoliosis/skeletal and spinal (CLOVES); megalencephaly-capillary malformation (MCAP or M-CM); fibro-adipose vascular anomaly (FAVA); Klippel-Trenaunay syndrome (KT; also known as, Klippel-Trenaunay-Weber syndrome); capillary, lymphatic, and venous malformations (CLVM); and lymphatic malformation (LM). …”
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    Qualitative research with patients and caregivers of patients with PIK3CA related overgrowth spectrum: content validity of clinical outcome assessments
  19. 1299
    “…The title compound was first reported by Luo, Yeh, Brossi, Flippen-Anderson & Gillardi [Helv. Chim. Acta (1984). 67, 1515–1522]. …”
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    Redetermination of dihydro­artemisinin at 103 (2) K
  20. 1300
    “…We describe an 8-year-old boy with developmental delay, clinical bilateral radial ulnar synostosis, Klippel-Feil anomaly, and other vertebral deformities who was found to have a de novo deletion of 114.5kb at 16p13.3. …”
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    Bilateral Radial Ulnar Synostosis and Vertebral Anomalies in a Child with a De Novo 16p13.3 Interstitial Deletion
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