Search Results - "Kharrat, K"

Refine Results
  1. 1

    Selecting the lowest instrumented vertebra in adolescent idiopathic scoliosis: Comparison of the Lenke, Suk, and Dubousset criteria by Rizkallah, M., Sebaaly, A., Kharrat, K., Kreichati, G.

    “…Selection of the lowest instrumented vertebra (LIV) in patients undergoing selective fusion for Lenke type 1 or 2 adolescent idiopathic scoliosis (AIS) varies…”
    Get full text
    Journal Article
  2. 2

    Fusionless surgery in early-onset scoliosis by Odent, T, Ilharreborde, B, Miladi, L, Khouri, N, Violas, P, Ouellet, J, Cunin, V, Kieffer, J, Kharrat, K, Accadbled, F

    “…Abstract Background Surgical treatment of early-onset scoliosis has greatly developed in recent years. Early-onset scoliosis covers a variety of etiologies…”
    Get full text
    Journal Article
  3. 3

    Fibrodysplasia ossificans progressiva: orthopedic pitfalls and controversies by Rachkidi, R, Ghanem, I, Dagher, F, Kharrat, K

    “…Fibrodysplasia ossificans progressiva (FOP) is a rare disorder of the connective tissue associating malformation of the great toes and progressive heterotopic…”
    Get full text
    Journal Article
  4. 4

    Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome by Hmani-Aifa, M, Arab, S Ben, Kharrat, K, Orten, D J, Boulila-Elgaied, A, Drira, M, Hachicha, S, Kimberling, W J, Ayadi, H

    Published in Journal of medical genetics (01-04-2002)
    “…According to a study performed in various ethnic populations, USH2A is responsible for more than 85% of USH2 cases. 9 This genetic form showed considerable…”
    Get full text
    Journal Article
  5. 5
  6. 6
  7. 7

    Fibrodysplasie ossifiante progressive : écueils orthopédiques et controverses by Rachkidi, R., Ghanem, I., Dagher, F., Kharrat, K.

    “…La fibrodysplasie ossifiante progressive (FOP) est une affection rare du tissu conjonctif associant une malformation des gros orteils et des ossifications…”
    Get full text
    Journal Article
  8. 8
  9. 9

    Four sibs with dislocated elbows, bowed tibiae, scoliosis, deafness, cataract, microcephaly, and mental retardation: a new MCA/MR syndrome by Mégarbané, A, Kharrat, K, Kreichati, G

    Published in Journal of medical genetics (01-09-1998)
    “…We report four sibs with an MCA/MR syndrome whose parents were first cousins. The sibs had mental retardation, microcephaly, hearing problems, cataract, and…”
    Get full text
    Journal Article
  10. 10

    Harrington instrumentation without fusion plus external orthotic support for the treatment of difficult curvature problems in young children by Moe, J H, Kharrat, K, Winter, R B, Cummine, J L

    Published in Clinical orthopaedics and related research (01-05-1984)
    “…In selected patients a method of rod insertion without fusion combined with use of a full-time external orthotic support, e.g., the Milwaukee brace, is…”
    Get more information
    Journal Article
  11. 11

    Adolescent bicipitoradial bursitis: a rare disease that can simulate a malignant tumor by Kheireddine, W, Ghanem, I, Dagher, F, Kharrat, K

    “…Bicipitoradial bursitis is a rare condition: we found 36 cases reported in the literature, none in children. The main manifestation is a painful tumefaction…”
    Get more information
    Journal Article
  12. 12
  13. 13

    Mirror hand deformity: a new phenotype with literature review by El Hage, S, Ghanem, I, Megarbané, A, Razzouk, C, Dagher, F, Kharrat, K

    “…We report the case of a child who presented polydactyly with eight triphalangeal fingers, no thumb or radius and ulnar dimelia. Hand, wrist, forearm and elbow…”
    Get more information
    Journal Article
  14. 14
  15. 15

    Computer-assisted surgery in total knee replacement. Preliminary results: report of 60 cases by El Masri, F, Rammal, H, Ghanem, I, El Hage, S, El Abiad, R, Kharrat, K, Dagher, F

    “…Conventional techniques proposed for total knee arthroplasty (TKA), necessarily require an acceptable alignment of the lower limb. Computer-assisted surgery is…”
    Get more information
    Journal Article
  16. 16

    Osteomyelitis of the rib due to Streptococcus pneumoniae: a very rare condition in children by Kalouche, Ibrahim, Ghanem, Ismat, Kharrat, Khalil, Dagher, Fernand

    Published in Journal of pediatric orthopaedics. B (01-01-2005)
    “…Rib osteomyelitis is a rare disease. We present a previously unreported case of Streptococcus pneumoniae osteomyelitis of the rib. A 4-month-old-infant…”
    Get full text
    Journal Article
  17. 17

    Percutaneous radiofrequency coagulation of osteoid osteoma in children and adolescents by Ghanem, Ismat, Collet, Louis-Michel, Kharrat, Khalil, Samaha, Elie, Deramon, Hervé, Mertl, Patrice, Dagher, Fernand

    Published in Journal of pediatric orthopaedics. B (01-07-2003)
    “…The purpose of this paper was to evaluate the effectiveness of percutaneous radiofrequency ablation of osteoid osteoma in children and adolescents…”
    Get full text
    Journal Article
  18. 18
  19. 19

    Recurrent Legg–Calvé–Perthes disease revisited: Fake or reality? by Ghanem, Ismat, Khalife, Rami, Haddad, Fadi, Kharrat, Khalil, Dagher, Fernand

    Published in Journal of pediatric orthopaedics. B (01-11-2005)
    “…The objective of this study was to assess the course, the epidemiologic features and the prognosis of recurrent Legg–Calvé–Perthes disease. We reviewed seven…”
    Get full text
    Journal Article
  20. 20

    Anesthetic management of a patient with Freeman-Sheldon syndrome: case report by Madi-Jebara, Samia, MD, El-Hajj, Christine, MD, Jawish, Dolly, MD, Ayoub, Eliane, MD, Kharrat, Khalil, MD, Antakly, Marie-Claire, MD

    Published in Journal of clinical anesthesia (01-09-2007)
    “…Abstract The Freeman-Sheldon syndrome (FSS) is a rare congenital myopathy and dysplasia. The musculoskeletal and soft-tissue manifestations of FSS often…”
    Get full text
    Journal Article