Rapid anti-secretory effects of glucocorticoids in human airway epithelium by Urbach, V., Verriere, V., Grumbach, Y., Bousquet, J., Harvey, B.J.

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RhoA GTPase regulates M-cadherin activity and myoblast fusion by Charrasse, Sophie, Comunale, Franck, Grumbach, Yaël, Poulat, Francis, Blangy, Anne, Gauthier-Rouvière, Cécile

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A new formula for correction of total calcium level into ionized serum calcium values in very elderly hospitalized patients by Pfitzenmeyer, Pierre, Martin, Isabelle, d’Athis, Philippe, Grumbach, Yolande, Delmestre, Marie-Claude, Blondé-Cynober, Françoise, Derycke, Béatrice, Brondel, Laurent

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For or against systematic screening of breast cancer before the age of fifty? by Grumbach, Y

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Pour ou contre le dépistage organisé du cancer du sein avant 50 ans ? by Grumbach, Y.

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BI-RADS, la nouvelle edition : conclusion by Grumbach, Y.

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La cytoponction echoguidee : quelle place en 2005 avec quels criteres de qualite by Baratte, B., Dehouck, I., Cognet, S., Grumbach, Y.

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Elastographie ultrasonore. Applications a la pathologie mammaire by Grumbach, Y., Baratte, B., Poirier, C., Cognet, S., Dehouck, I.

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Le controle de qualite des ponctions echoguidees by Grumbach, Y., Baratte, B., Cognet, S., Dehouck, I., Poirier, C.

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Metaphyseal anadysplasia in two sisters by SLAMA, M, MATHIEU, M, DEHOUCK, I, AL HOSRI, J, VANTHOURNOUT, I, BARATTE, B, GRUMBACH, Y

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PRAGMATIQUE, SITUATION D'ÉNONCIATION ET DEIXIS by Wunderlich, Dieter, Grumbach, Jenny

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DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4) by Chen, Ying-Zhang, Bennett, Craig L., Huynh, Huy M., Blair, Ian P., Puls, Imke, Irobi, Joy, Dierick, Ines, Abel, Annette, Kennerson, Marina L., Rabin, Bruce A., Nicholson, Garth A., Auer-Grumbach, Michaela, Wagner, Klaus, De Jonghe, Peter, Griffin, John W., Fischbeck, Kenneth H., Timmerman, Vincent, Cornblath, David R., Chance, Phillip F.

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Reentrant multiple-q magnetic order and a “spin meta-cholesteric” phase in Sr3Fe2O7 by Andriushin, N. D., Muller, J., Pavlovskii, N. S., Grumbach, J., Granovsky, S., Tymoshenko, Y. V., Zaharko, O., Ivanov, A., Ollivier, J., Doerr, M., Keimer, B., Mostovoy, M., Inosov, D. S., Peets, D. C.

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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia by Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Müller, Juliane S, Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M, Alfares, Ahmed A, Zhu, Changlian, Uhrova Meszarosova, Anna, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R, Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T, Strom, Tim M, De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P, Portier, Ruben, Bergmann, Carsten, Ghasemi Firouzabadi, Saghar, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A, Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W, Tran Mau-Them, Frederic, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laëtitia, Schmitt, Emmanuelle, Lacaze, Elodie, Küpper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J H, Grand, Katheryn, Graham, John M, Lewis, Richard A, Millan, Francisca, Duman, Özgür, Dündar, Nihal, Uyanik, Gökhan, Schöls, Ludger, Nürnberg, Peter, Nürnberg, Gudrun, Catala Bordes, Andrea, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Bouçanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S, Shamseldin, Hanan, Al Tala, Saeed, Rezazadeh Varaghchi, Jamileh, Najafi, Maryam, Deschner, Selina, Gläser, Dieter, Hüttel, Wolfgang, Kruer, Michael C, Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Züchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schüle, Rebecca, Horvath, Rita

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Genetic spectrum of hereditary neuropathies with onset in the first year of life by Baets, Jonathan, Deconinck, Tine, De Vriendt, Els, Zimo, Magdalena, Yperzeele, Laetitia, Van Hoorenbeeck, Kim, Peeters, Kristien, Spiegel, Ronen, Parman, Yesim, Ceulemans, Berten, Van Bogaert, Patrick, Pou-Serradell, Adolf, Bernert, Günther, Dinopoulos, Argirios, Auer-Grumbach, Michaela, Sallinen, Satu-Leena, Fabrizi, Gian Maria, Pauly, Fernand, Van den Bergh, Peter, Bilir, Birdal, Battaloglu, Esra, Madrid, Ricardo E., Kabzi ska, Dagmara, Kochanski, Andrzej, Topaloglu, Haluk, Miller, Geoffrey, Jordanova, Albena, Timmerman, Vincent, De Jonghe, Peter

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Molecular Basis of Aromatase Deficiency in an Adult Female with Sexual Infantilism and Polycystic Ovaries by Ito, Yuji, Fisher, Carolyn R., Conte, Felix A., Grumbach, Melvin M., Simpson, Evan R.

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Differential Control of Calcium Homeostasis and Vascular Reactivity by Ca2+/Calmodulin-Dependent Kinase II by Prasad, Anand M, Nuno, Daniel W, Koval, Olha M, Ketsawatsomkron, Pimonrat, Li, Weiwei, Li, Hui, Shen, Fred Y, Joiner, Mei-ling A, Kutschke, William, Weiss, Robert M, Sigmund, Curt D, Anderson, Mark E, Lamping, Kathryn G, Grumbach, Isabella M

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Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies by Lischka, Annette, Eggermann, Katja, Record, Christopher J, Dohrn, Maike F, Laššuthová, Petra, Kraft, Florian, Begemann, Matthias, Dey, Daniela, Eggermann, Thomas, Beijer, Danique, Šoukalová, Jana, Laura, Matilde, Rossor, Alexander M, Mazanec, Radim, Van Lent, Jonas, Tomaselli, Pedro J, Ungelenk, Martin, Debus, Karlien Y, Feely, Shawna M E, Gläser, Dieter, Jagadeesh, Sujatha, Martin, Madelena, Govindaraj, Geeta M, Singhi, Pratibha, Baineni, Revanth, Biswal, Niranjan, Ibarra-Ramírez, Marisol, Bonduelle, Maryse, Gess, Burkhard, Romero Sánchez, Juan, Suthar, Renu, Udani, Vrajesh, Nalini, Atchayaram, Unnikrishnan, Gopikrishnan, Marques, Junior, Wilson, Mercier, Sandra, Procaccio, Vincent, Bris, Céline, Suresh, Beena, Reddy, Vaishnavi, Skorupinska, Mariola, Bonello-Palot, Nathalie, Mochel, Fanny, Dahl, Georg, Sasidharan, Karthika, Devassikutty, Fiji M, Nampoothiri, Sheela, Rodovalho Doriqui, Maria J, Müller-Felber, Wolfgang, Vill, Katharina, Haack, Tobias B, Dufke, Andreas, Abele, Michael, Stucka, Rolf, Siddiqi, Saima, Ullah, Noor, Spranger, Stephanie, Chiabrando, Deborah, Bolgül, Behiye S, Parman, Yesim, Seeman, Pavel, Lampert, Angelika, Schulz, Jörg B, Wood, John N, Cox, James J, Auer-Grumbach, Michaela, Timmerman, Vincent, de Winter, Jonathan, Themistocleous, Andreas C, Shy, Michael, Bennett, David L, Baets, Jonathan, Hübner, Christian A, Leipold, Enrico, Züchner, Stephan, Elbracht, Miriam, Çakar, Arman, Senderek, Jan, Hornemann, Thorsten, Woods, C Geoffrey, Reilly, Mary M, Kurth, Ingo

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Genetics of Pain: Novel variants identified by the European Network on Inherited Sensory Neuropathies and Insensitivity to Pain (ENISNIP) by Lischka, A, Eggermann, K, Cakar, A, Bocek, R, Bartesaghi, L, Elbracht, M, Hornemann, T, Senderek, J, Auer-Grumbach, M, Parman, Y, Lassuthova, P, Kurth, I

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Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology by Berenbaum, S, Chrousos, G, Clayton, P, Cutler, G, Keizer-Schrama, SD, Donahoe, PK, Donahoue, PA, Donaldson, M, Forest, M, Fujieda, K, Ghionizz, L, Ginalska-Malinowska, M, Grumbach, MM, Gruters, A, Hagenfeldt, K, Hintz, RL, Honour, JW, Hughes, IA, Kuhnle-Krahl, U, Lee, PA, Meyer-Bahlburg, H, Migeon, C, Miller, WL, Muller, J, New, MI, Oberfield, SE, Peter, M, Ritzen, EM, Saenger, P, Savage, MO, Schober, JM, Sippell, WG, Solyom, J, Speiser, PW, Therrell, BL, Van Wyk, JJ, Warne, GL, White, PC, Wildt, L, Witchell, S, Hindmarsh, PC, Holmes, LB, Ibanez, L, Levine, LS, Pang, SY, Wedell, A

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