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Clinical Dysmorphology, ISSN 0962-8827, 01/2012, Volume 21, Issue 1, pp. 19 - 21
Pycnodysostosis (OMIM 265800) is an uncommon hereditary disorder characterized by osteosclerosis of the skeleton, short stature, and bone fragility. The... 
GENETICS & HEREDITY | Facial Bones - abnormalities | Craniosynostoses - genetics | Humans | Skull - abnormalities | Pycnodysostosis - genetics | Male | Pycnodysostosis - pathology | Child | Genes, Recessive | Craniosynostoses - pathology | Craniofacial Dysostosis - genetics | Index Medicus
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2015, Volume 74, Issue 6, pp. 1019 - 1023
Journal Article
by Pons-Estel, Bernardo A and Bonfa, Eloisa and Soriano, Enrique R and Cardiel, Mario H and Izcovich, Ariel and Popoff, Federico and Criniti, Juan M and Vásquez, Gloria and Massardo, Loreto and Duarte, Margarita and Barile-Fabris, Leonor A and García, Mercedes A and Amigo, Mary-Carmen and Espada, Graciela and Catoggio, Luis J and Sato, Emilia Inoue and Levy, Roger A and Acevedo Vásquez, Eduardo M and Chacón-Díaz, Rosa and Galarza-Maldonado, Claudio M and Iglesias Gamarra, Antonio J and Molina, José Fernando and Neira, Oscar and Silva, Clóvis A and Vargas Peña, Andrea and Gómez-Puerta, José A and Scolnik, Marina and Pons-Estel, Guillermo J and Ugolini-Lopes, Michelle R and Savio, Verónica and Drenkard, Cristina and Alvarellos, Alejandro J and Ugarte-Gil, Manuel F and Babini, Alejandra and Cavalcanti, André and Cardoso Linhares, Fernanda Athayde and Haye Salinas, Maria Jezabel and Fuentes-Silva, Yurilis J and Montandon de Oliveira e Silva, Ana Carolina and Eraso Garnica, Ruth M and Herrera Uribe, Sebastián and Gómez-Martín, Diana and Robaina Sevrini, Ricardo and Quintana, Rosana M and Gordon, Sergio and Fragoso-Loyo, Hilda and Rosario, Violeta and Saurit, Verónica and Appenzeller, Simone and dos Reis Neto, Edgard Torres and Cieza, Jorge and González Naranjo, Luis A and González Bello, Yelitza C and Collado, María Victoria and Sarano, Judith and Retamozo, Soledad and Sattler, María E and Gamboa-Cárdenas, Rocio V and Cairoli, Ernesto and Conti, Silvana M and Amezcua-Guerra, Luis M and Silveira, Luis H and Borba, Eduardo F and Pera, Mariana A and Alba Moreyra, Paula B and Arturi, Valeria and Berbotto, Guillermo A and Gerling, Cristian and Gobbi, Carla A and Gervasoni, Viviana L and Scherbarth, Hugo R and Brenol, João C Tavares and Cavalcanti, Fernando and Costallat, Lilian T Lavras and Da Silva, Nilzio A and Monticielo, Odirlei A and Seguro, Luciana Parente Costa and Xavier, Ricardo M and Llanos, Carolina and Montúfar Guardado, Rubén A and Garcia de la Torre, Ignacio and Pineda, Carlos and Portela Hernández, Margarita and Danza, Alvaro and Guibert-Toledano, Marlene and Reyes, Gil Llerena and Acosta Colman, Maria Isabel and Aquino, Alicia M and Mora-Trujillo, Claudia S and Muñoz-Louis, Roberto and García Valladares, Ignacio and Orozco, María Celeste and Burgos, Paula I and Betancur, Graciela V and Alarcón, Graciela S and Grp Latino Amer Estudio Lupus and Pan-Amer League Assoc Rheumatology and Grupo Latino Americano de Estudio del Lupus (GLADEL) and Pan-American League of Associations of Rheumatology (PANLAR)
Annals of the Rheumatic Diseases, ISSN 0003-4967, 11/2018, Volume 77, Issue 11, pp. 1549 - 1557
Systemic lupus erythematosus (SLE), a complex and heterogeneous autoimmune disease, represents a significant challenge for both diagnosis and treatment.... 
treatment | lupus nephritis | systemic lupus erythematosus | HYDROXYCHLOROQUINE | MORTALITY | MANAGEMENT | INCEPTION COHORT | DISEASE | RISK | RHEUMATOLOGY | 3 ETHNIC-GROUPS | COLLEGE-OF-RHEUMATOLOGY | ANCESTRY | DAMAGE | Lupus | Anticoagulants | Aspirin | Systemic lupus erythematosus | Glucocorticoids | Rheumatology | Socio-economic aspects | Rituximab | Arthritis | Patients | Antiphospholipid syndrome | 1506 | 2311 | Recommendation
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2019, Volume 1922, pp. 453 - 492
This chapter describes methods related to the diagnosis of genetic dental diseases. Based on the present knowledge, clinical phenotyping and next-generation... 
Epigenetics | Cell culture | Next-generation sequencing | Tooth agenesis | Amelogenesis imperfecta | Dentin inherited disorders | Index Medicus
Journal Article
Revista Universitas Medica, ISSN 0041-9095, 07/2013, Volume 54, Issue 3, pp. 385 - 395
La incontinencia es una patologia frecuente que afecta de manera relevante a las mujeres. La incomodidad fisica que ocasiona y los inconvenientes asociados... 
Urinary incontinence
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 03/2016, Volume 31, Issue 3, pp. 498 - 513
Journal Article
Journal of Dentistry for Children, ISSN 1551-8949, 01/2010, Volume 77, Issue 1, pp. 36 - 41
Journal Article
Journal Article