7 results on '"Razzouk, M."'
Search Results
2. Paralysie du plexus brachial obstétrical C5-8 : stratégie chirurgicale et résultats
- Author
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Lombard, A., primary, Bachy-Razzouk, M., additional, and Fitoussi, F.N., additional
- Published
- 2019
- Full Text
- View/download PDF
3. Poster display IV experimental and instrumentation
- Author
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Masoli, O., Redruello, M., Ogresta, F., Collaud, C., Koslowski, P., Baliño, N., Eleta, M., Arce, P., Vidal, L., Kardash, O., Maroz-Vadalajskaya, N., Vanhove, C., Lahoutte, T., Defrise, M., Andreyev, A., Bossuyt, A., Franken, P., Maskali, F., Nloga, J., Tran, N., Marie, P., Peix, A., Garcia-Barreto, D., Ponce, F., Cabrera, L., Valiente, J., Tornes, F., Guerrero, I., Heres, F., Garcia, E., Cabale, B., Bindslev, L., Bisgaard, K., Haack-Soerensen, M., Mortensen, S., Kragh, L., Kjaer, A., Kastrup, J., Hesse, B., Aboul-Enein, F., Battah, A., Fattah, A., Atty, A., Allam, A., Riou, L., Broisat, A., Ghezzi, C., Lartizien, C., Berthonneche, C., Toufektsian, M., Maitrejean, S., Janier, M., Vanzetto, G., Fagret, D., Rouzet, F., Daou, D., Lebtahi, R., Frank, R., Leenhardt, A., Slama, M., Guludec, D., Sarda-Mantel, L., Michel, J., Martet, G., Meulemans, A., Vrigneaud, J., Coaguila, C., Benada, A., Razzouk, M., Idy-Peretti, I., Vilain, D., Stegger, L., Schäfers, K., Flögel, U., Schrader, J., Schober, O., Levkau, B., Schäfers, M., Kies, P., Wichter, T., Wielepp, J., Baller, D., Pulawski, E., Weise, R., Fricke, E., Horstkotte, D., Burchert, W., Eckert, S., Dongas, A., Nekolla, S., Martinez, M., Howe, W., Kehren, F., Ziegler, S., Vassiliadis, I., Souretis, G., Komporozos, C., Fountos, A., Papademetriou, A., Spanos, A., Antoniou, A., Strembelas, P., Moralidis, E., Arsos, G., Boundas, D., Georga, S., Karatzas, N., Karakatsanis, K., Prassopoulos, V., Parthenakis, F., Patrianakos, A., Koukouraki, S., Velidaki, A., Karkavitsas, N., Vardas, P., Perisinakis, K., Koutsikos, J., Sundaraiya, S., Sumati, S., Sambhasivam, KA, David, S., Zakavi, S., Kakhki, V., Jabari, H., Zingerman, B., Bendayan, D., Sagie, A., Solodky, A., Mats, I., Shapira, Y., Kremer, M., Zafrir, N., Rimini, M., Catalano, M., Bonzani, G., Scalzone, A., Merenda, R., Monteforte, I., Monda, V., Muto, P., Carboni, G., Miglionico, M., Tavolozza, M., Marcassa, C., Campini, R., Calza, P., Giannuzzi, P., Eleuteri, E., Scapellato, F., Temporelli, P., Pellegrino, T., Storto, G., Sorrentino, A., Silvestri, A., Filardi, P., Brevetti, G., Cuocolo, A., Cho, K., Kumita, S., Seino, K., Nakajo, H., Toba, M., Kumazaki, T., Muramatsu, T., Yamazaki, T., Seki, K., Kawanami, J., Nakajima, T., Yamada, Y., Suga, T., Matsumoto, K., Nishimura, S., Taki, J., Higuchi, T., Kawashima, A., Nakajima, K., Muramori, A., Matsunari, I., Tait, J., Vanderheyden, J., Strauss, H., Tonami, N., Adachi, I., Shimomura, H., Kintaka, T., Komori, T., Ogura, Y., Kitaura, Y., Narabayashi, I., Iida, H., Zeniya, T., Kim, K., Watabe, H., Teramoto, N., Yamamichi, Y., Alexanderson, E., Ricalde, A., Vargas, A., Meave, A., Amigo, M., Misko, J., Dziuk, M., Warczynska, A., Skrobowska, E., Vasconcelos, M., Martins, E., Faria, T., Oliveira, A., Pardal, N., Macedo, F., Pereira, J., Rocha-Gonçalves, F., Cantinho, G., Pena, H., Freire, L., Veiga, A., Gonçalves, P., Godinho, F., Chua, T., Lee, C., Keng, F., Ding, Z., Koh, T., Awamleh, P., Talavera, P., Torres, V., Balsa, M., González, O., Alberca, M., Miguel, R., Cosío, F., Lomsky, M., Richter, J., Johansson, L., El-Ali, H., Åström, K., Ljungberg, M., Edenbrandt, L., Hung, G., Lee, K., Chen, C., Yang, K., Pekindil, G., Sarikaya, A., Ege, T., Salihoglu, S., Entok, E., Cavusoglu, Y., Ak, I., Vardareli, E., Timuralp, B., Tout, D., Loong, C., Naidoo, V., Aswegen, A., Underwood, S., Thorley, P., Goris, M., ZHU, H., Clements, I., Mullan, B., O'Connor, M., Breen, J., McGregor, C., Liu, Y., Li, S., Bourke, B., Weyman, C., Sinusas, A., Ramakrishna, G., Miller, T., Gibbons, R., Tsatkin, V., Wackers, F., Prior, J., Facta, A., Schindler, T., Oxilia-Estigarribia, M., Hernandez-Pampaloni, M., Campisi, R., Zhang, X., Bischof-Delaloye, A., Nathan, L., Schelbert, H., Gullberg, G., Huesman, R., Reutter, B., Sitek, A., Veress, A., Weiss, J., Qi, J., Yang, Y., Gordi, T., Olmsted, A., Lieu, H., Belardinelli, L., Masoli, O., Redruello, M., Ogresta, F., Collaud, C., Koslowski, P., Baliño, N., Eleta, M., Arce, P., Vidal, L., Kardash, O., Maroz-Vadalajskaya, N., Vanhove, C., Lahoutte, T., Defrise, M., Andreyev, A., Bossuyt, A., Franken, P., Maskali, F., Nloga, J., Tran, N., Marie, P., Peix, A., Garcia-Barreto, D., Ponce, F., Cabrera, L., Valiente, J., Tornes, F., Guerrero, I., Heres, F., Garcia, E., Cabale, B., Bindslev, L., Bisgaard, K., Haack-Soerensen, M., Mortensen, S., Kragh, L., Kjaer, A., Kastrup, J., Hesse, B., Aboul-Enein, F., Battah, A., Fattah, A., Atty, A., Allam, A., Riou, L., Broisat, A., Ghezzi, C., Lartizien, C., Berthonneche, C., Toufektsian, M., Maitrejean, S., Janier, M., Vanzetto, G., Fagret, D., Rouzet, F., Daou, D., Lebtahi, R., Frank, R., Leenhardt, A., Slama, M., Guludec, D., Sarda-Mantel, L., Michel, J., Martet, G., Meulemans, A., Vrigneaud, J., Coaguila, C., Benada, A., Razzouk, M., Idy-Peretti, I., Vilain, D., Stegger, L., Schäfers, K., Flögel, U., Schrader, J., Schober, O., Levkau, B., Schäfers, M., Kies, P., Wichter, T., Wielepp, J., Baller, D., Pulawski, E., Weise, R., Fricke, E., Horstkotte, D., Burchert, W., Eckert, S., Dongas, A., Nekolla, S., Martinez, M., Howe, W., Kehren, F., Ziegler, S., Vassiliadis, I., Souretis, G., Komporozos, C., Fountos, A., Papademetriou, A., Spanos, A., Antoniou, A., Strembelas, P., Moralidis, E., Arsos, G., Boundas, D., Georga, S., Karatzas, N., Karakatsanis, K., Prassopoulos, V., Parthenakis, F., Patrianakos, A., Koukouraki, S., Velidaki, A., Karkavitsas, N., Vardas, P., Perisinakis, K., Koutsikos, J., Sundaraiya, S., Sumati, S., Sambhasivam, KA, David, S., Zakavi, S., Kakhki, V., Jabari, H., Zingerman, B., Bendayan, D., Sagie, A., Solodky, A., Mats, I., Shapira, Y., Kremer, M., Zafrir, N., Rimini, M., Catalano, M., Bonzani, G., Scalzone, A., Merenda, R., Monteforte, I., Monda, V., Muto, P., Carboni, G., Miglionico, M., Tavolozza, M., Marcassa, C., Campini, R., Calza, P., Giannuzzi, P., Eleuteri, E., Scapellato, F., Temporelli, P., Pellegrino, T., Storto, G., Sorrentino, A., Silvestri, A., Filardi, P., Brevetti, G., Cuocolo, A., Cho, K., Kumita, S., Seino, K., Nakajo, H., Toba, M., Kumazaki, T., Muramatsu, T., Yamazaki, T., Seki, K., Kawanami, J., Nakajima, T., Yamada, Y., Suga, T., Matsumoto, K., Nishimura, S., Taki, J., Higuchi, T., Kawashima, A., Nakajima, K., Muramori, A., Matsunari, I., Tait, J., Vanderheyden, J., Strauss, H., Tonami, N., Adachi, I., Shimomura, H., Kintaka, T., Komori, T., Ogura, Y., Kitaura, Y., Narabayashi, I., Iida, H., Zeniya, T., Kim, K., Watabe, H., Teramoto, N., Yamamichi, Y., Alexanderson, E., Ricalde, A., Vargas, A., Meave, A., Amigo, M., Misko, J., Dziuk, M., Warczynska, A., Skrobowska, E., Vasconcelos, M., Martins, E., Faria, T., Oliveira, A., Pardal, N., Macedo, F., Pereira, J., Rocha-Gonçalves, F., Cantinho, G., Pena, H., Freire, L., Veiga, A., Gonçalves, P., Godinho, F., Chua, T., Lee, C., Keng, F., Ding, Z., Koh, T., Awamleh, P., Talavera, P., Torres, V., Balsa, M., González, O., Alberca, M., Miguel, R., Cosío, F., Lomsky, M., Richter, J., Johansson, L., El-Ali, H., Åström, K., Ljungberg, M., Edenbrandt, L., Hung, G., Lee, K., Chen, C., Yang, K., Pekindil, G., Sarikaya, A., Ege, T., Salihoglu, S., Entok, E., Cavusoglu, Y., Ak, I., Vardareli, E., Timuralp, B., Tout, D., Loong, C., Naidoo, V., Aswegen, A., Underwood, S., Thorley, P., Goris, M., ZHU, H., Clements, I., Mullan, B., O'Connor, M., Breen, J., McGregor, C., Liu, Y., Li, S., Bourke, B., Weyman, C., Sinusas, A., Ramakrishna, G., Miller, T., Gibbons, R., Tsatkin, V., Wackers, F., Prior, J., Facta, A., Schindler, T., Oxilia-Estigarribia, M., Hernandez-Pampaloni, M., Campisi, R., Zhang, X., Bischof-Delaloye, A., Nathan, L., Schelbert, H., Gullberg, G., Huesman, R., Reutter, B., Sitek, A., Veress, A., Weiss, J., Qi, J., Yang, Y., Gordi, T., Olmsted, A., Lieu, H., and Belardinelli, L.
- Published
- 2018
4. [Fractures in children: epidemiological, diagnostic and therapeutic features].
- Author
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Gaume M, Thouement C, Vialle R, and Bachy-Razzouk M
- Abstract
Competing Interests: Les auteurs déclarent n'avoir aucun lien d'intérêts.
- Published
- 2024
5. Analysis of a Chronic Lateral Ankle Instability Model in the Rat: Conclusions and Suggestions for Future Research.
- Author
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Saliba I, Bachy-Razzouk M, Bensidhoum M, Hoc T, Potier E, Vialle R, and Hardy A
- Abstract
The purpose of this study was to evaluate potential osteoarthritic alterations within the ankle using a surgically-induced chronic lateral ankle instability (CLAI) model. Twelve rats were assigned randomly to either the control ( n = 4) or CLAI group ( n = 8). Surgery was performed on the right ankle. Osteoarthritis was assessed through in-vivo micro-CT at 8 weeks and a clinical analysis. Macroscopic analysis, high-resolution ex-vivo micro-CT and histological examination were conducted after euthanasia at 12 weeks. Three subgroups (SG) were analyzed. SG1 comprised the operated ankles of the CLAI group ( n = 8). SG2 consisted of the non-operated ankles of the CLAI group ( n = 8). SG3 included both sides of the control group ( n = 8). In-vivo micro-CT revealed no significant differences among the three subgroups when analyzed together ( p = 0.42), and when comparing SG1 with SG2 ( p = 0.23) and SG3 ( p = 0.43) individually. No noticeable clinical differences were observed. After euthanasia, macroscopic analysis employing OARSI score, did not demonstrate significant differences, except between the medial tibia of SG1 and SG3 ( p = 0.03), and in the total score comparison between these two subgroups ( p = 0.015). Ex-vivo micro-CT did not reveal any differences between the three subgroups regarding bony irregularities and BV/TV measurements (SG1 vs. SG2 vs. SG3: p = 0.72; SG1 vs. SG2: p = 0.80; SG1 vs. SG3: p = 0.72). Finally, there was no difference between the three subgroups regarding OARSI histologic score ( p = 0.27). These findings indicate that the current model failed to induce significant osteoarthritis. However, they lay the groundwork for improving the model's effectiveness and expanding its use in CLAI research, aiming to enhance understanding of this pathology and reduce unnecessary animal sacrifice.
- Published
- 2024
- Full Text
- View/download PDF
6. Correlation between histopathological nerve assessment and clinical recovery in brachial plexus birth injuries.
- Author
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Moulinier C, Bellity L, Saghbiny E, Bachy-Razzouk M, Hanneur ML, and Fitoussi F
- Subjects
- Humans, Male, Female, Brachial Plexus Neuropathies surgery, Brachial Plexus Neuropathies physiopathology, Range of Motion, Articular, Fibrosis, Spinal Nerve Roots surgery, Spinal Nerve Roots injuries, Infant, Child, Preschool, Child, Adolescent, Recovery of Function, Birth Injuries surgery, Birth Injuries complications, Brachial Plexus injuries, Brachial Plexus surgery
- Abstract
In the management of brachial plexus birth palsies, the quality of the roots eligible for reconstruction is thought to be a key issue. The aim of the present study was to evaluate the correlations between pathological root examination and motor recovery after brachial plexus reconstructions. Quantitative histopathological analysis of intraneural fibrosis was conducted on 72 nerve transections (40 roots, 18 trunks and 14 suprascapular nerves) in 20 patients. Clinical recovery of targeted muscles after surgery was assessed by standardized functional scores. After a mean follow-up of 32 months, patients with a lower fibrosis rate for the suprascapular nerve had greater global Mallet scores (r = -0.57; p = 0.042) as well as a greater active shoulder flexion (r = -0.66; p = 0.015). Correlations were also found between C6 root and upper trunk fibrosis rate and some of the subsections of the Mallet score, active movement scale for the biceps and active elbow flexion. These results seem to confirm the relevance of intraoperative pathological evaluation of the roots and nerves after neuroma resection to optimally define the reconstruction strategy. Level of evidence: IV., Competing Interests: Declaration of conflicting interestsThe authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
- Published
- 2024
- Full Text
- View/download PDF
7. In Vivo Assessment of Skin Surface Pattern: Exploring Its Potential as an Indicator of Bone Biomechanical Properties.
- Author
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Aurégan JC, Bosser C, Bachy-Razzouk M, Bensidhoum M, and Hoc T
- Abstract
The mechanical properties of bone tissue are the result of a complex process involving collagen-crystal interactions. The mineral density of the bone tissue is correlated with bone strength, whereas the characteristics of collagen are often associated with the ductility and toughness of the bone. From a clinical perspective, bone mineral density alone does not satisfactorily explain skeletal fragility. However, reliable in vivo markers of collagen quality that can be easily used in clinical practice are not available. Hence, the objective of the present study is to examine the relationship between skin surface morphology and changes in the mechanical properties of the bone. An experimental study was conducted on healthy children (n = 11), children with osteogenesis imperfecta (n = 13), and women over 60 years of age (n = 22). For each patient, the skin characteristic length (SCL) of the forearm skin surface was measured. The SCL quantifies the geometric patterns formed by wrinkles on the skin's surface, both in terms of size and elongation. The greater the SCL, the more deficient was the organic collagen matrix. In addition, the bone volume fraction and mechanical properties of the explanted femoral head were determined for the elderly female group. The mean SCL values of the healthy children group were significantly lower than those of the elderly women and osteogenesis imperfecta groups. For the aged women group, no significant differences were indicated in the elastic mechanical parameters, whereas bone toughness and ductility decreased significantly as the SCL increased. In conclusion, in bone collagen pathology or bone aging, the SCL is significantly impaired. This in vivo skin surface parameter can be a non-invasive tool to improve the estimation of bone matrix quality and to identify subjects at high risk of bone fracture.
- Published
- 2023
- Full Text
- View/download PDF
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