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  1. 1301
    “…We demonstrate that two GDF6 prodomain mutants linked to Klippel-Feil syndrome are hyperactive in CD99-Src signaling. …”
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    GDF6-CD99 Signaling Regulates Src and Ewing Sarcoma Growth
  2. 1302
    “…Cervical radiographs were suggestive of Klippel-Feil syndrome. The chiropractor suspected a vascular cause such as a transient ischemic attack and referred the patient to the emergency department, which the patient visited the following day. …”
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    An Adult Patient With Acute Ischemic Stroke and Carotid Stenosis Presenting to a Chiropractor: A Case Report
  3. 1303
    “…Using an independent software program, we confirmed (for the complex biological endpoint of carcinogenicity) the validity of a structure-activity relationship approach of the type proposed by Klopman and Rosenkranz with their CASE program.…”
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    Relationship between molecular connectivity and carcinogenic activity: a confirmation with a new software program based on graph theory.
  4. 1304
    “…One patient was a 6-year-old girl weighing 12.7 kg and had Klippel-Feil syndrome with Arnold-Chiari malformation, the other was a 24-year-old female weighing 31 kg and had juvenile rheumatoid arthritis. …”
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    Fiberoptic intubation through a laryngeal mask airway as a management of difficult airwary due to the fusion of the entire cervical spine - A report of two cases -
  5. 1305
    “…Angiogenic factor with G-patch and FHA domain 1 (AGGF1) is a novel angiogenic factor that was first described in Klippel-Trenaunay syndrome, a congenital vascular disease associated with capillary and venous malformations. …”
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    Angiogenic Factor with G-patch and FHA Domain 1 (AGGF1) Expression in Human Vascular Lesions
  6. 1306
    por Robles, Luis A.
    Publicado 2017
    “…CASE DESCRIPTION: Following a motor vehicle accident, a 25-year-old female's radiographic studies showed an oblique axis fracture involving both the anterior and posterior elements along with an anterior and posterior Klippel–Feil syndrome (KFS) anomaly. Following treatment in a halo vest, the patient maintained alignment, and ultimately the fracture was fused. …”
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    True oblique axis fracture associated with congenital anomalies of the upper cervical spine: Case report of an unusual fracture pattern
  7. 1307
    “…Although rather recalcitrant to treatment, topical agents such as hydroquinone, modified Kligman's Regime, azelaic acid, kojic acid, Vitamin C, and arbutin still remain the mainstay of therapy with sun protection being a cornerstone of therapy. …”
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    Medical Management of Melasma: A Review with Consensus Recommendations by Indian Pigmentary Expert Group
  8. 1308
    por Chernoff, Egan J.
    Publicado 2021
    “…Knowing this little factoid, imagine my horror when it recently dawned on me that, no matter where I looked during this COVID-19 pandemic, all I saw was flippant treatment towards the metric system. As I detail in this article, COVID-19 social distancing signage, here in Canada, presents indifference towards the metric system. …”
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    The Metre as a Metric: Canada’s COVID-19 Conversion Kerfuffle
  9. 1309
    “…After conducting radiological studies, he was diagnosed with medullary neuroschisis without pontine malformations and Klippel-Feil syndrome with rib anomalies. Based on these findings, we propose that clinical AMDC can be accompanied by a wide variety of musculoskeletal defects and variable degrees of central nervous system malformations. …”
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    A Wide Spectrum of Axial Mesodermal Dysplasia Complex With Rhombencephalic Anomaly: A Case Report
  10. 1310
    “…LK(6)C showed low allergenic potential and failed to provoke any sensitivity when administered to guinea pigs in the Magnusson-Kligman maximization test. When applied topically as a dressing, the medium-infused LK(6)C hydrogel accelerated re-epithelialization compared to controls. …”
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    Transparent crosslinked ultrashort peptide hydrogel dressing with high shape-fidelity accelerates healing of full-thickness excision wounds
  11. 1311
    “…A 33-week pregnant patient with Klippel-Trenaunay syndrome, past SARS-CoV-2 infection and type I fetal growth restriction with shortening of the fetal long bone was diagnosed in our center with a probable CAPS. …”
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    Catastrophic antiphospholipid syndrome during pregnancy
  12. 1312
    “…Open-source firmware by Klipper and Fluidd is used for control. The printer is able to reach 500 °C nozzle, 200 °C heated bed, and 135 °C heated chamber with all electronics inside operating within the recommended temperature range. …”
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    High-performance polymer 3D printing – Open-source liquid cooled scalable printer design
  13. 1313
    “…The polymers were then hydrolyzed using a commercial lipase from Thermomyces lanuginosus (Lipopan(®) 50 BG). A higher degradation rate was found for the polymers prepared using Lactol-citro molecules, compared to those obtained by the polycondensation reactions of diacyl chlorides with Triol-citro—a monomer recently obtained by the selective reduction of HBO-citro.…”
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    Synthesis and Enzymatic Degradation of Sustainable Levoglucosenone-Derived Copolyesters with Renewable Citronellol Side Chains
  14. 1314
    “…PIK3CA variants were found in 67% of Klippel Trenaunay Syndrome individuals; KRAS variants in 60% of arteriovenous malformations; MET was mutated in 75% of lymphovenous malformations. …”
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    Nosological and Theranostic Approach to Vascular Malformation through cfDNA NGS Liquid Biopsy
  15. 1315
    “…INTRODUCTION AND IMPORTANCE: Servelle-Martorell syndrome (SMS) is a rare congenital anomaly that is frequently mistaken for Klippel-Trenaunay syndrome (KTS) or Parkes-Weber syndrome (PWS). …”
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    A rare case report of a Servelle-Martorell syndrome patient
  16. 1316
    “…Finally, the metaphors exhibit a flippant tone that seems inappropriate for a serious discussion of health science.…”
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    Deconstructing anti-harm-reduction metaphors; mortality risk from falls and other traumatic injuries compared to smokeless tobacco use
  17. 1317
    “…In addition, mutations in BMP13 have recently been associated with Klippel-Feil Syndrome, causative of numerous skeletal and developmental defects including spinal disc fusion. …”
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    Unveiling the Bmp13 Enigma: Redundant Morphogen or Crucial Regulator?
  18. 1318
    “…In the light of a recent report that mutations in the BMP-13 gene are associated with spine vertebral fusion in Klippel-Feil syndrome, we hypothesized that BMP-13 signaling is crucial for regulating embryonic endochondral ossification. …”
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    BMP-13 Emerges as a Potential Inhibitor of Bone Formation
  19. 1319
    “…Increased growth is also seen in neurofibromatosis, hemangiomatosis, arteriovenous malformations, congenital lymphedema, and syndromes such as Klippel–Trenaunay–Weber syndrome and Proteus syndrome. …”
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    Island nail flap in the treatment of foot macrodactyly of the first ray in children: report of two cases
  20. 1320
    “…Missense mutations in Growth/Differentiation Factor 3 (GDF3) gene have previously been reported in patients with microphthalmia, iridial and retinal colobomas, Klippel-Feil anomaly with vertebral fusion, scoliosis, rudimentary 12th ribs and an anomalous right temporal bone. …”
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    A recurrent, non-penetrant sequence variant, p.Arg266Cys in Growth/Differentiation Factor 3 (GDF3) in a female with unilateral anophthalmia and skeletal anomalies
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