Increased Leptin/Adiponectin Ratio and Free Leptin Index Are Markers of Insulin Resistance in Obese Girls during Pubertal Development von Donoso, M.A., Muñoz-Calvo, M.T., Barrios, V., Martínez, G., Hawkins, F., Argente, J.

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Increased circulating adiponectin levels and decreased leptin/soluble leptin receptor ratio throughout puberty in female ballet dancers: association with body composition and the d... von Donoso, M A, Muñoz-Calvo, M T, Barrios, V, Garrido, G, Hawkins, F, Argente, J

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Genetic analysis of BRCA1 and BRCA2 in breast/ovarian cancer families from Aragon (Spain): two novel truncating mutations and a large genomic deletion in BRCA1 von Miramar, M. D., Calvo, M. T., Rodriguez, A., Antón, A., Lorente, F., Barrio, E., Herrero, A., Burriel, J., García de Jalón, A.

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Maintained malnutrition produces a progressive decrease in (OPG) RANKL ratio and leptin levels in patients with anorexia nervosa von Muñoz-Calvo, M. T., Barrios, V., GarcÍa de Álvaro, M. T., Lefort, M., Méndez-Dávila, C., Argente, J., de la Piedra, C.

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Treatment of Palmar Hyperhidrosis by Peripheral Nerve Block at the Wrist With Botulinum Toxin von de Quintana-Sancho, A., Calvo, M.T. Conde

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Association of BRCA1 germline mutations in young onset triple-negative breast cancer (TNBC) von Andrés, R., Pajares, I., Balmaña, J., Llort, G., Ramón y Cajal, T., Chirivella, I., Aguirre, E., Robles, L., Lastra, E., Pérez-Segura, P., Bosch, N., Yagüe, C., Lerma, E., Godino, J., Miramar, M. D., Moros, M., Astier, P., Saez, B., Vidal, M. J., Arcusa, A., Ramón y Cajal, S., Calvo, M. T., Tres, A.

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Clinical and radiological findings in a case of pseudohypoparathyroidism type 1a. Albright hereditary osteodystrophy von Sanz-Fernández, M, Muñoz-Calvo, M T, Pozo-Román, J, Martos-Moreno, G A, Argente, J

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Discrepant factor VIII activity in a family with mild haemophilia A and 531 mutation using various FVIII assays and APTT reagents von Lucía, J F, Aguilar, C, Dobon, M, Aznar, J A, Tizano, E, Borés, C, Cornudella, R, Calvo, M T

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4CPS-170 Evaluation of zoledronic acid in the treatment of bone diseases with high risk of fractures von Puivecino-Moreno, C, Alcalá-Soto, A, Vázquez-Vela, V, Jiménez-Pichardo, L, Varas-Pérez, A, Marín-Ariza, I, Gómez-de-Travecedo-Calvo, MT

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Severe polyarthritis as a rare adverse effect associated with methimazole therapy in a patient with Graves' disease von Caballero Mora, F J, Muñoz Calvo, M T, López Robledillo, J C, Argente, J

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Wine Volatile and Amino Acid Composition after Malolactic Fermentation:  Effect of Oenococcus oeni and Lactobacillus plantarum Starter Cultures von Pozo-Bayón, M. A, G-Alegría, E, Polo, M. C, Tenorio, C, Martín-Álvarez, P. J, Calvo de la Banda, M. T, Ruiz-Larrea, F, Moreno-Arribas, M. V

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Different expression of the Asn264LysfsX35 mutation of the GNAS gene in a family with pseudohypoparathyroidism. von de Arriba Muñoz, A, Labarta Aizpún, J I, Dehesa, E Mayayo, Calvo, M T, Pérez de Nanclares, G, Ferrández-Longás, A

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Cervical cancer screening in Spain von Fernández Calvo, M.T, Hernández Rubio, A, Rosell Aguilar, I

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First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene von Domènech, Enric, Kruyer, Helena, Gómez, Carolina, Calvo, Maria Teresa, Nunes, Virginia

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4CPS-119 Pneumonology-pharmacy collaboration in the pharmacotherapeutic optimisation of monoclonal antibodies in patients with severe uncontrolled asthma von Alcala Soto, A, Pérez Grimaldi, F, Soto Campos, JG, Cuadros Martínez, CM, Gómez de Travecedo Y Calvo, MT, Sierra Sánchez, JF

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Three novel mutations (P215L, T289P, and 3811-2 A→G) in the rhodopsin gene in autosomal dominant retinitis pigmentosa in Spanish families von Martinez-Gimeno, María, Trujillo, María José, Lorda, Isabel, Gimenez, Ascensión, Calvo, María Teresa, Ayuso, Carmen, Carballo, Miguel

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Treatment of Palmar Hyperhidrosis by Peripheral Nerve Block at the Wrist With Botulinum Toxin von de Quintana-Sancho, A, Conde Calvo, M T

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Trends in the treatment of dermatophytosis von Del Palacio, A, Garau, M, Gonzalez-Escalada, A, Calvo, M T

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New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism von Fernández-Rebollo, Eduardo, Lecumberri, Beatriz, Garin, Intza, Arroyo, Javier, Bernal-Chico, Ana, Goñi, Fernando, Orduña, Rosa, Castaño, Luis, Pérez de Nanclares, Guiomar

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Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at the GNAS Locus von Perez-Nanclares, Gustavo, Romanelli, Valeria, Mayo, Sonia, Garin, Intza, Zazo, Celia, Fernandez-Rebollo, Eduardo, Martínez, Francisco, Lapunzina, Pablo, de Nanclares, Guiomar Pérez, the Spanish PHP Group

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