Works matching DE "MUSCLE dysmorphia"

Results: 367

Evaluating the reliability and validity of the proposed muscle dysmorphia criteria.

Published in:

International Journal of Sport & Exercise Psychology, 2016, v. 14, n. 3, p. 195, doi. 10.1080/1612197X.2015.1016088

By:

Nieuwoudt, Johanna Elizabeth;
Zhou, Shi;
Coutts, Rosanne;
Booker, Ray;
Yoxall, Jacqui;
Booker, Samantha

Publication type:

Article

Walker-Warburg syndrome.

Published in:

2018

By:

Suthar, Renu;
Angurana, Suresh K;
Singh, Usha;
Singh, Paramjeet

Publication type:

journal article

Identification of microdeletion and microduplication syndromes by chromosomal microarray in patients with intellectual disability with dysmorphism.

Published in:

2018

By:

Panigrahi, Inusha;
Jain, Puneet;
Didel, Siyaram;
Agarwal, Sarita;
Muthuswamy, Srinivasan;
Saha, Ansuman;
Kulkarni, Vinay

Publication type:

journal article

Implications on IVF patient care of discarding oocytes affected by smooth endoplasmic reticulum aggregates as recommended by the Alpha/ESHRE consensus.

Published in:

2015

By:

Shaw-Jackson, Chloë

Publication type:

Letter

Polar body fragmentation in IVM oocytes is associated with impaired fertilization and embryo development.

Published in:

Journal of Assisted Reproduction & Genetics, 2013, v. 30, n. 5, p. 679, doi. 10.1007/s10815-013-9982-4

By:

Rose, B.;
Laky, D.

Publication type:

Article

Bilateral arcuate foramen associated with partial defect of the posterior arch of the atlas in a medieval skeleton: case report and review of the literature. Looking backward to go forward.

Published in:

Surgical & Radiologic Anatomy, 2011, v. 33, n. 6, p. 495, doi. 10.1007/s00276-010-0760-z

By:

Travan, Luciana;
Saccheri, Paola;
Sabbadini, Gastone;
Crivellato, Enrico

Publication type:

Article

The Effects of Different Pressure Types on the Development of Muscle Dysmorphia in High School Students.

Published in:

Journal of the Kentucky Academy of Science, 2023, v. 84, n. 1, p. 31, doi. 10.3101/kyac-84-01-02

By:

Mullick, Alisha;
Grieve, Frederick G.

Publication type:

Article

Detection of Muscle Dysmorphia symptoms in male weightlifters.

Published in:

Anales de Psicología, 2017, v. 33, n. 1, p. 204, doi. 10.6018/analesps.33.1.233311

By:

Hemández-Martínez, Andrea;
González-Martí, Irene;
Contreras Jordán, Onofre Ricardo

Publication type:

Article

Evaluación diagnóstica de la Dismorfia Muscular: una revisión sistemática.

Published in:

Anales de Psicología, 2016, v. 32, n. 2, p. 405, doi. 10.6018/analesps.32.2.203871

By:

Lopez-Cuautle, Camilo;
Vazquez-Arevalo, Rosalia;
Mancilla-Díaz, Juan Manuel

Publication type:

Article

Eating- and Weight-Related Disorders in the Armed Forces.

Published in:

Metabolites (2218-1989), 2024, v. 14, n. 12, p. 667, doi. 10.3390/metabo14120667

By:

Himmerich, Hubertus;
Gravina, Davide;
Schalinski, Inga;
Willmund, Gerd-Dieter;
Zimmermann, Peter Lutz;
Keeler, Johanna Louise;
Treasure, Janet

Publication type:

Article

Appearance Teasing and Mental Health: Gender Differences and Mediation Effects of Appearance-Based Rejection Sensitivity and Dysmorphic Concerns.

Published in:

Frontiers in Psychology, 2019, p. N.PAG, doi. 10.3389/fpsyg.2019.00579

By:

Schmidt, Jennifer;
Martin, Alexandra

Publication type:

Article

Understanding Appearance- Enhancing Drug Use in Sport Using an Enactive Approach to Body Image.

Published in:

Frontiers in Psychology, 2017, p. 1, doi. 10.3389/fpsyg.2017.02088

By:

Hauw, Denis;
Bilard, Jean

Publication type:

Article

Comment on “Original Solution for Middle Ear Implant and Anesthetic/Surgical Management in a Child with Severe Craniofacial Dysmorphism”.

Published in:

Case Reports in Otolaryngology, 2016, p. 1, doi. 10.1155/2016/2859051

By:

Kruyt, Ivo Joachim;
Mc Dermott, Ann-Louise;
Hol, Myrthe Karianne Sophie

Publication type:

Article

Recombinant chromosome 4 resulting from a maternal pericentric inversion in two sisters presenting consistent dysmorphic features.

Published in:

2007

By:

Stembalska, Agnieszka;
Laczmanska, Izabela;
Schlade-Bartusiak, Kamila;
Czemarmazowicz, Halina;
Murawski, Marek;
Sasiadek, Maria

Publication type:

journal article

Kabuki Syndrome—Clinical Review with Molecular Aspects.

Published in:

Genes, 2021, v. 12, n. 4, p. 468, doi. 10.3390/genes12040468

By:

Boniel, Snir;
Szymańska, Krystyna;
Śmigiel, Robert;
Szczałuba, Krzysztof

Publication type:

Article

Pitt-Hopkins Syndrome: Clinical and Molecular Findings of a 5-Year-Old Patient.

Published in:

Genes, 2020, v. 11, n. 6, p. 596, doi. 10.3390/genes11060596

By:

Tripon, Florin;
Bogliș, Alina;
Micheu, Cristian;
Streață, Ioana;
Bănescu, Claudia

Publication type:

Article

Muscle dysmorphia: what about transgender people?

Published in:

Culture, Health & Sexuality, 2022, v. 24, n. 1, p. 63, doi. 10.1080/13691058.2020.1814968

By:

Amodeo, Anna Lisa;
Esposito, Concetta;
Antuoni, Sabrina;
Saracco, Giovanni;
Bacchini, Dario

Publication type:

Article

Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome.

Published in:

2010

By:

Colarusso, Gloria;
Gambineri, Eleonora;
Lapi, Elisabetta;
Casini, Tommaso;
Tucci, Fabio;
Lippi, Francesca;
Azzari, Chiara

Publication type:

Case Study

Clinical and molecular characterization of a patient with a combination of a deletion and a duplication of 22q13 using array CGH.

Published in:

Application of Clinical Genetics, 2012, v. 5, p. 93, doi. 10.2147/TACG.S35799

By:

Ochando, Isabel;
Urbano, Antonio;
Rubio, Juana;
Rueda, Joaquín

Publication type:

Article

A dependência pela prática de exercícios físicos e o uso de recursos ergogênicos.

Published in:

Acta Scientiarum: Health Sciences, 2010, v. 32, n. 1, p. 35, doi. 10.4025/actascihealthsci.v32i1.4475

By:

Vieira, José Luiz Lopes;
da Rocha, Priscila Garcia Marques;
Ferrarezzi, Ricardo Aparecido

Publication type:

Article

Role of Phosphoinositide-Specific Phospholipase C η2 in Isolated and Syndromic Mental Retardation.

Published in:

European Neurology, 2011, v. 65, n. 5, p. 264, doi. 10.1159/000327307

By:

Lo Vasco, Vincenza Rita

Publication type:

Article

The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation.

Published in:

Molecular Cytogenetics (17558166), 2015, v. 8, p. 106, doi. 10.1186/s13039-015-0205-9

By:

Fonseca, Ana Carolina S.;
Bonaldi, Adriano;
Fonseca, Simone A. S.;
Otto, Paulo A.;
Kok, Fernando;
Bak, Mads;
Tommerup, Niels;
Vianna-Morgante, Angela M.

Publication type:

Article

Complex chromosomal aberrations in a fetus originating from oocytes with smooth endoplasmic reticulum (SER) aggregates.

Published in:

Systems Biology in Reproductive Medicine, 2018, v. 64, n. 4, p. 283, doi. 10.1080/19396368.2018.1466375

By:

Sfontouris, Ioannis A.;
Lainas, George T.;
Lainas, Tryfon G.;
Faros, Efthimios;
Banti, Maria;
Kardara, Katerina;
Anagnostopoulou, Katerina;
Kontos, Harris;
Petsas, George K.;
Kolibianakis, Efstratios M.

Publication type:

Article

Muscle Dysmorphic Disorder Inventory (MDDI): Validation of a German version with a focus on gender.

Published in:

PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0207535

By:

Zeeck, Almut;
Welter, Viola;
Alatas, Hasan;
Hildebrandt, Tom;
Lahmann, Claas;
Hartmann, Armin

Publication type:

Article

Reevaluation of Physique Protection as a Characteristic of Muscle Dysmorphia.

Published in:

North American Journal of Psychology, 2014, v. 16, n. 3, p. 575

By:

Baghurst, Timothy;
Mwavita, Mwarumba;
Volberding, Jennifer;
Brown, Theresa C.;
Murray, Stuart B.;
Galli, Nick;
Parish, Anthony;
Griffiths, Scott

Publication type:

Article

Brief Report on Men's Bodies and Mood: Correlates between Depressive Symptoms and Muscle Dysmorphia Symptoms.

Published in:

North American Journal of Psychology, 2012, v. 14, n. 3, p. 563

By:

Grieve, Frederick G.;
Shacklette, Michael D.

Publication type:

Article

Exposure to Male Models in Advertisements Leads to a Decrease in Men's Body Satisfaction.

Published in:

North American Journal of Psychology, 2006, v. 8, n. 1, p. 115

By:

Baird, Amy L.;
Grieve, Frederick G.

Publication type:

Article

Are extremes of consumption in eating disorders related to an altered balance between reward and inhibition?

Published in:

Frontiers in Behavioral Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fnbeh.2014.00410

By:

Wierenga, Christina E.;
Ely, Alice;
Bischoff-Grethe, Amanda;
Bailer, Ursula F.;
Simmons, Alan N.;
Kaye, Walter H.

Publication type:

Article

Kidney disease associated with androgenic-anabolic steroids and vitamin supplements abuse: Be aware!

Published in:

Nefrologia, 2020, v. 40, n. 1, p. 26, doi. 10.1016/j.nefro.2019.06.003

By:

Arruda Parente Filho, Sérgio Luiz;
Andrade de Carvalho Gomes, Pedro Eduardo;
Aguiar Forte, Guilherme;
Lopes Lima, Laio Ladislau;
Bezerra da Silva Júnior, Geraldo;
Cavalcante Meneses, Gdayllon;
Maria Costa Martins, Alice;
De Francesco Daher, Elizabeth

Publication type:

Article

1q44 microdeletion syndrome: A new case with potential additional features.

Published in:

Romanian Journal of Medical Practice, 2021, v. 16, n. 1, p. 92, doi. 10.37897/RJMP.2021.1.16

By:

SHELBY, Elena-Silvia;
HUSEYINOGLU, Tanser;
CARDOS, Georgeta;
PADURE, Liliana;
MIREA, Andrada;
LEANCA, Madalina;
BADINA, Mihaela;
BARLADEANU, Nadejda;
NEDELEA, Florina Mihaela

Publication type:

Article

Congenital myasthenic syndromes.

Published in:

2019

By:

Finsterer, Josef

Publication type:

journal article

A restricted spectrum of NRAS mutations causes Noonan syndrome.

Published in:

Nature Genetics, 2010, v. 42, n. 1, p. 27, doi. 10.1038/ng.497

By:

Cirstea, Ion C.;
Kutsche, Kerstin;
Dvorsky, Radovan;
Gremer, Lothar;
Carta, Claudio;
Horn, Denise;
Roberts, Amy E.;
Lepri, Francesca;
Merbitz-Zahradnik, Torsten;
König, Rainer;
Kratz, Christian P.;
Pantaleoni, Francesca;
Dentici, Maria L.;
Joshi, Victoria A.;
Kucherlapati, Raju S.;
Mazzanti, Laura;
Mundlos, Stefan;
Patton, Michael A.;
Silengo, Margherita Cirillo;
Rossi, Cesare

Publication type:

Article

Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

Published in:

Nature Genetics, 2007, v. 39, n. 1, p. 75, doi. 10.1038/ng1939

By:

Tartaglia, Marco;
Pennacchio, Len A.;
Zhao, Chen;
Yadav, Kamlesh K.;
Fodale, Valentina;
Sarkozy, Anna;
Pandit, Bhaswati;
Oishi, Kimihiko;
Martinelli, Simone;
Schackwitz, Wendy;
Ustaszewska, Anna;
Martin, Joel;
Bristow, James;
Carta, Claudio;
Lepri, Francesca;
Neri, Cinzia;
Vasta, Isabella;
Gibson, Kate;
Curry, Cynthia J.;
Siguero, Juan Pedro López

Publication type:

Article

Tetralogy of Fallot and hypertrophic cardiomyopathy in a case of cardiofaciocutaneous syndrome.

Published in:

Turkish Journal of Pediatrics, 2008, v. 50, n. 3, p. 275

By:

Yıldırım, Selman Vefa;
Kale-Çekinmez, Eren;
Özcan, Deren;
Derbent, Murat

Publication type:

Article

Angelman syndrome: clinical findings and follow-up data of 14 patients.

Published in:

Turkish Journal of Pediatrics, 2008, v. 50, n. 2, p. 137

By:

Kara, Bülent;
Karaman, Birsen;
Özmen, Meral;
Rosti, Rasim Özgür;
Çalişkan, Mine;
Kayserili, Hülya;
Başaran, Seher

Publication type:

Article

Muscle dysmorphia: detection of the use-abuse of anabolic androgenic steroids in a Spanish sample.

Published in:

Adicciones, 2018, v. 30, n. 4, p. 243

By:

GONZÁLEZ-MARTÍ, IRENE;
FERNÁNDEZ-BUSTOS, JUAN GREGORIO;
CONTRERAS JORDÁN, ONOFRE RICARDO;
SOKOLOVA, MARINA

Publication type:

Article

Two GNPTAB Variations Caused Mucolipidosis II Alpha/Beta in a Chinese Family.

Published in:

Fetal & Pediatric Pathology, 2025, v. 44, n. 2, p. 157, doi. 10.1080/15513815.2025.2466057

By:

Yang, Jingxin;
Liu, Chao;
Geng, Qian;
Chen, Liyuan;
Zhang, Lei;
Wu, Weiqing

Publication type:

Article

Detection of ocular hypertelorism among Indian children.

Published in:

Indian Journal of Medical Research, 2022, v. 155, n. 3/4, p. 364, doi. 10.4103/ijmr.IJMR_758_20

By:

Bhalla, Anil Kumar;
Kaur, Harvinder;
Kaur, Rupinder

Publication type:

Article

Novel ATRX gene damaging missense mutation c.6740A>C segregates with profound to severe intellectual deficiency without alpha thalassaemia.

Published in:

Indian Journal of Medical Research, 2016, v. 143, n. 1, p. 43, doi. 10.4103/0971-5916.178589

By:

Bouazzi, Habib;
Thakur, Seema;
Trujillo, Carlos;
Alwasiyah, Mohammad Khalid;
Munnich, Arnold

Publication type:

Article

Muscle Dysmorphia, Gender Role Stress, and Sociocultural Influences: An Exploratory Study.

Published in:

Research Quarterly for Exercise & Sport, 2011, v. 82, n. 2, p. 310, doi. 10.5641/027013611X13119541884103

By:

Readdy, Tucker;
Watkins, Patti Lou;
Cardinal, Bradley J.

Publication type:

Article

A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism.

Published in:

Cytogenetic & Genome Research, 2015, v. 145, n. 1, p. 1, doi. 10.1159/000381234

By:

del Refugio Rivera-Vega, Maria;
Gómez-del angel, Luis a.;
Valdes-Miranda, Juan M.;
Pérez-Cabrera, adrián;
Gonzalez-Huerta, Luz M.;
Toral-López, Jaime;
Cuevas-Covarrubias, Sergio

Publication type:

Article

An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review.

Published in:

Cytogenetic & Genome Research, 2014, v. 142, n. 4, p. 227, doi. 10.1159/000361001

By:

Vlaikou, angeliki-Maria;
Manolakos, Emmanouil;
Noutsopoulos, Dimitrios;
Markopoulos, Georgios;
Liehr, Thomas;
Vetro, annalisa;
Ziegler, Monika;
Weise, anja;
Kreskowski, Katharina;
Papoulidis, Ioannis;
Thomaidis, Loretta;
Syrrou, Maria

Publication type:

Article

Unique Genomic Structure and Distinct Mitotic Behavior of Ring Chromosome 21 in Two Unrelated Cases.

Published in:

Cytogenetic & Genome Research, 2012, v. 136, n. 3, p. 180, doi. 10.1159/000336978

By:

Zhang, H.Z.;
Xu, F.;
Seashore, M.;
Li, P.

Publication type:

Article

Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects.

Published in:

Cytogenetic & Genome Research, 2011, v. 135, n. 3/4, p. 251, doi. 10.1159/000331272

By:

Breckpot, J.;
Thienpont, B.;
Arens, Y.;
Tranchevent, L.C.;
Vermeesch, J.R.;
Moreau, Y.;
Gewillig, M.;
Devriendt, K.

Publication type:

Article

Clinical and Molecular Characterization of a Combined 17p13.3 Microdeletion with Partial Monosomy 21q21.3 in a 26-Year-Old Man.

Published in:

Cytogenetic & Genome Research, 2011, v. 135, n. 2, p. 102, doi. 10.1159/000330880

By:

Hannachi, H.;
Mougou-Zerelli, S.;
BenAbdallah, I.;
Mama, N.;
Hamdi, I.;
Labalme, A.;
Elghezal, H.;
Sanlaville, D.;
Saad, A.

Publication type:

Article

Severe Phenotype in a Girl with Partial Tetrasomy 7, Karyotype 46,XX,trp(7)(q35q36).

Published in:

Cytogenetic & Genome Research, 2009, v. 125, n. 3, p. 248, doi. 10.1159/000230009

By:

Lehnen, H.;
Maiwald, R.;
Neyzen, S.;
Kohlhase, J.;
Böhm, D.;
Ritterbach, J.;
Behrend, C.;
Schwennicke, G.

Publication type:

Article

Kir 2.1 channelopathies: the Andersen–Tawil syndrome.

Published in:

Pflügers Archiv: European Journal of Physiology, 2010, v. 460, n. 2, p. 289, doi. 10.1007/s00424-010-0820-6

By:

Tristani-Firouzi, Martin;
Etheridge, Susan P.

Publication type:

Article

Navigation and 3D-imaging in pelvic ring surgery: a systematic review of prospective comparative studies.

Published in:

Archives of Orthopaedic & Trauma Surgery, 2024, v. 144, n. 10, p. 4549, doi. 10.1007/s00402-024-05468-2

By:

Boudissa, Mehdi;
Khoury, Georges;
Franke, Jochen;
Gänsslen, Axel;
Tonetti, Jérôme

Publication type:

Article

Iliac dysmorphism: defining radiographic characteristics and association with pelvic osseous corridor size.

Published in:

Archives of Orthopaedic & Trauma Surgery, 2023, v. 143, n. 4, p. 1841, doi. 10.1007/s00402-022-04376-7

By:

Wang, Miqi;
Jacobs, Robert C.;
Bartlett, Craig S.;
Schottel, Patrick C.

Publication type:

Article

The dark side of bodybuilding: the role of bodybuilding activities in compensation of frustrated basic psychological needs.

Published in:

Motivation & Emotion, 2020, v. 44, n. 2, p. 190, doi. 10.1007/s11031-019-09805-6

By:

Selvi, Kerim;
Bozo, Özlem

Publication type:

Article