Works matching DE "AMELOGENESIS imperfecta"

Results: 450

Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel ROGDI Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz Syndrome.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 705, doi. 10.1111/cge.14725

By:

Essid, Miriam;
Karoui, Sana;
Zribi, Mouna;
Ben Younes, Thouraya;
Januel, Louis;
Lafont, Estelle;
Labalme, Audrey;
Ben Hafsa, Meriem;
Hun Seo, Go;
Khatrouch, Safa;
Boudabous, Hela;
Ben Chehida, Amel;
Sanlaville, Damien;
Jilani, Houweyda;
Benjemaa, Lamia;
Kraoua, Ichraf;
Lesca, Gaetan;
Chatron, Nicolas

Publication type:

Article

A novel mutation in CNNM4 is associated with a case of Jalili syndrome in Egypt.

Published in:

2025

By:

Tawfik, Caroline Atef;
Aly, Haneen Sabry;
Kabeel, Menna;
Yousri, Iman;
Mohamed, Sara Abdallah

Publication type:

Case Study

Towards a Modernized Framework of Histology Teaching to Integrate Genetics: Pedagogical Perspectives for Oral Histology.

Published in:

Genes, 2025, v. 16, n. 5, p. 512, doi. 10.3390/genes16050512

By:

Kristoffersen, Camilla Sofia Miranda;
Ziesler, Camilla Elise Øxnevad;
Thune, Noora Helene;
Kristensen, Anna Tostrup;
Sehic, Amer;
Utheim, Tor Paaske;
Khan, Qalbi

Publication type:

Article

Challenges of Studying Amelogenesis in Gene-Targeted Mouse Models.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 10, p. 4905, doi. 10.3390/ijms26104905

By:

Smith, Charles E.;
Bartlett, John D.;
Simmer, James P.;
Hu, Jan C.-C.

Publication type:

Article

Effects of Deproteinization on Bond Strength of Composite to Primary Teeth Affected by Amelogenesis.

Published in:

Pediatric Dentistry, 2019, v. 41, n. 4, p. 304

By:

Bayrak, Sule;
Tuloglu, Nuray;
Tune, Emine Sen

Publication type:

Article

Dental Management of Heritable Dental Developmental Anomalies.

Published in:: Pediatric Dentistry, 2017, v. 39, n. 6, p. 348
Publication type:: Article

Guideline on Dental Management of Heritable Dental Developmental Anomalies.

Published in:: 2016
Publication type:: journal article

Molecular characterization of the Yp11.2 region deletion in the Chinese Han population.

Published in:

International Journal of Legal Medicine, 2021, v. 135, n. 4, p. 1351, doi. 10.1007/s00414-021-02596-x

By:

Pang, Qianqian;
Lin, Qingai;
Wang, Di;
Sun, Zhenghao;
Wang, Junfang

Publication type:

Article

Çukurova Popülasyonunda Gelişimsel Diş Anomalisi Görülme Sıklığı: Radyografik Bir Çalışma.

Published in:

Selcuk Dental Journal, 2023, v. 10, n. 2, p. 434, doi. 10.15311/selcukdentj.1168337

By:

SÜSGÜN YILDIRIM, Zehra;
EVLİCE, Burcu;
SONKAYA, Ezgi

Publication type:

Article

Corrections of Dental Anomalies in the Maxillary Incisors and Their Influence on Perceived Smile Esthetics: A Systematic Review.

Published in:

Bioengineering (Basel), 2025, v. 12, n. 3, p. 262, doi. 10.3390/bioengineering12030262

By:

McGarty, Nessa Rose;
Delre, Caterina;
Gaeta, Carlo;
Doldo, Tiziana

Publication type:

Article

Interdisciplinary Approach of Amelogenesis Imperfecta: 10 Years of Clinical Follow-Up.

Published in:

Journal of Health Sciences (2447-8938), 2021, v. 23, n. 1, p. 18, doi. 10.17921/2447-8938.2021v23n1p18-24

By:

Toma, Mauro;
Rico Bocato, Jessica;
Magno Goshe, Carlos;
Teixeira Borsato, Thais;
de Castro Ferreira Conti, Ana Claúdia;
Freire Fernandes, Thais Maria;
Pedron Oltramari, Paula Vanessa

Publication type:

Article

Crowning glory.

Published in:

Biologist, 2014, v. 61, n. 6, p. 16

By:

Poulter, James

Publication type:

Article

Growth and Overall Health of Patients with SLC13A5 Citrate Transporter Disorder.

Published in:

Metabolites (2218-1989), 2021, v. 11, n. 11, p. 746, doi. 10.3390/metabo11110746

By:

Brown, Tanya L.;
Nye, Kimberly L.;
Porter, Brenda E.

Publication type:

Article

Genetic evaluation of paediatric nephrocalcinosis: phenotype-driven genetic panels reveal a rare diagnosis.

Published in:

Clinical Kidney Journal, 2022, v. 15, n. 4, p. 812, doi. 10.1093/ckj/sfab279

By:

Patterson, Jenny;
Jacob, Zoe;
Reynolds, Ben C

Publication type:

Article

A suitable method.

Published in:

British Dental Journal, 2012, v. 213, n. 5, p. 198, doi. 10.1038/sj.bdj.2012.785

By:

Prasanna, T. R.;
Sachin, G.

Publication type:

Article

The interdisciplinary management of patients with amelogenesis imperfecta - restorative dentistry.

Published in:

British Dental Journal, 2012, v. 212, n. 11, p. 537, doi. 10.1038/sj.bdj.2012.469

By:

Malik, K.;
Gadhia, K.;
Arkutu, N.;
McDonald, S.;
Blair, F.

Publication type:

Article

Amelogenesis imperfecta: the orthodontic perspective.

Published in:

British Dental Journal, 2012, v. 212, n. 10, p. 485, doi. 10.1038/sj.bdj.2012.415

By:

Arkutu, N.;
Gadhia, K.;
McDonald, S.;
Malik, K.;
Currie, L.

Publication type:

Article

Managing the paediatric patient with amelogenesis imperfecta.

Published in:

British Dental Journal, 2012, v. 212, n. 9, p. 425, doi. 10.1038/sj.bdj.2012.366

By:

McDonald, S.;
Arkutu, N.;
Malik, K.;
Gadhia, K.;
McKaig, S.

Publication type:

Article

Amelogenesis imperfecta: an introduction.

Published in:

British Dental Journal, 2012, v. 212, n. 8, p. 377, doi. 10.1038/sj.bdj.2012.314

By:

Gadhia, K.;
McDonald, S.;
Arkutu, N.;
Malik, K.

Publication type:

Article

SCREW RETAINED IMPLANT SUPPORTED PROSTHESIS.

Published in:: 2012
Publication type:: Case Study

AMELOGENESIS IMPERFECTA.

Published in:

Guident, 2012, v. 5, n. 8, p. 84

By:

Kamala, K. A.;
Guddad, Sanketh S.

Publication type:

Article

AMELOGENESIS IMPERFECTA AND ITS IMPLICATIONS IN ORTHODONTICS.

Published in:

Guident, 2012, v. 5, n. 4, p. 35

By:

Shenava, Shailesh;
Sankar, Hanumanth;
Samuel, Soumi

Publication type:

Article

An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature.

Published in:

Genes, 2022, v. 13, n. 7, p. 1272, doi. 10.3390/genes13071272

By:

Leban, Tina;
Trebušak Podkrajšek, Katarina;
Kovač, Jernej;
Fidler, Aleš;
Pavlič, Alenka

Publication type:

Article

A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3.

Published in:

2021

By:

Flex, Elisabetta;
Imperatore, Valentina;
Carpentieri, Giovanna;
Bruselles, Alessandro;
Ciolfi, Andrea;
Pizzi, Simone;
Tedesco, Maria Giovanna;
Rogaia, Daniela;
Mencarelli, Amedea;
Di Cara, Giuseppe;
Verrotti, Alberto;
Troiani, Stefania;
Merla, Giuseppe;
Tartaglia, Marco;
Prontera, Paolo

Publication type:

Case Study

Identification of a Homozygous PEX26 Mutation in a Heimler Syndrome Patient.

Published in:

Genes, 2021, v. 12, n. 5, p. 646, doi. 10.3390/genes12050646

By:

Kim, Youn Jung;
Abe, Yuichi;
Kim, Young-Jae;
Fujiki, Yukio;
Kim, Jung-Wook;
Crisponi, Laura

Publication type:

Article

A Novel De Novo SP6 Mutation Causes Severe Hypoplastic Amelogenesis Imperfecta.

Published in:

Genes, 2021, v. 12, n. 3, p. 346, doi. 10.3390/genes12030346

By:

Kim, Youn Jung;
Lee, Yejin;
Zhang, Hong;
Song, Ji-Soo;
Hu, Jan C.-C.;
Simmer, James P.;
Kim, Jung-Wook;
Crisponi, Laura

Publication type:

Article

Dental developmental disturbances in 50 individuals with the 22q11.2 deletion syndrome; relation to medical conditions?

Published in:

Acta Odontologica Scandinavica, 2012, v. 70, n. 3, p. 194, doi. 10.3109/00016357.2011.629624

By:

Nordgarden, Hilde;
Lima, Kari;
Skogedal, Nina;
Følling, Ivar;
Storhaug, Kari;
Abrahamsen, Tore G.

Publication type:

Article

A multidisciplinary approach for the diagnosis of hypocalcified amelogenesis imperfecta in two Chilean families.

Published in:

Acta Odontologica Scandinavica, 2012, v. 70, n. 1, p. 7, doi. 10.3109/00016357.2011.574973

By:

Urzúa, Blanca;
Ortega-Pinto, Ana;
Farias, Daniela Adorno;
Franco, Eugenia;
Morales-Bozo, Irene;
Moncada, Gustavo;
Escobar-Pezoa, Nicolás;
Scholz, Ursula;
Cifuentes, Victor

Publication type:

Article

Prevalence and distribution of selected dental anomalies in the patients reporting to dental institute, RIMS, Ranchi.

Published in:

Journal of Pharmacy & Bioallied Sciences, 2021, v. 13, p. 993, doi. 10.4103/jpbs.jpbs_148_21

By:

Mohan, Sumit;
Viswanath, Butta;
Thakur, Jyoti;
Tekriwal, Shweta;
Singh, Anubhuti;
Jaiswal, Rima

Publication type:

Article

Prevalence and Distribution of Selected Dental Anomalies in the Patients Reporting to Dental Institute, RIMS, Ranchi.

Published in:

Journal of Pharmacy & Bioallied Sciences, 2021, v. 13, p. 993, doi. 10.4103/jpbs.jpbs_148_21

By:

Mohan, Sumit;
Viswanath, Butta;
Thakur, Jyoti;
Tekriwal, Shweta;
Singh, Anubhuti;
Jaiswal, Rima

Publication type:

Article

Amelogenesis imperfecta and endodontic treatment: report of two cases.

Published in:

Endodontic Practice Today, 2020, v. 14, n. 1, p. 63

By:

Schäfer, Magdalena;
Donnermeyer, David;
Schäfer, Edgar

Publication type:

Article

Immunohistochemical Study of Amelogenin Binding Proteins in an Amelogenin Point Mutation Mouse.

Published in:

International Journal of Morphology, 2019, v. 37, n. 2, p. 522, doi. 10.4067/S0717-95022019000200522

By:

Naoko Otawa-Kamogashira;
Yuko Matsuda;
Masaaki Takezaki;
Yuji Hatakeyama;
Sachio Tamaoki;
Hiroyuki Ishikawa

Publication type:

Article

A Novel Homozygous 9385 bp Deletion in the FERMT1 (KIND1) Gene in a Malaysian Family with Kindler Epidermolysis bullosa and a Review of Large Deletions.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 9, p. 4237, doi. 10.3390/ijms26094237

By:

Klausegger, Alfred;
Leditzky, Fabian;
Krämer, Susanne;
Palisson, Francis;
Yubero, María Joao;
Véliz, Sebastián;
Koh, Mark Jean Aan;
Tan, Ene-Choo;
Laimer, Martin;
Bauer, Johann Wolfgang;
Fuentes, Ignacia

Publication type:

Article

Association between developmental dental anomalies, early childhood caries and oral hygiene status of 3–5-year-old children in Ile-Ife, Nigeria.

Published in:

BMC Oral Health, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12903-019-0991-2

By:

Folayan, Morenike Oluwatoyin;
Alade, Michael;
Adeniyi, Abiola;
El Tantawi, Maha;
Finlayson, Tracy L.

Publication type:

Article

Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports.

Published in:

BMC Oral Health, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12903-018-0554-y

By:

Toupenay, Steve;
Fournier, Benjamin Philippe;
Manière, Marie-Cécile;
Ifi-Naulin, Chantal;
Berdal, Ariane;
de La Dure– Molla, Muriel

Publication type:

Article

IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta.

Published in:

PLoS Genetics, 2025, v. 21, n. 1, p. 1, doi. 10.1371/journal.pgen.1011328

By:

Hytönen, Marjo K.;
Rönkkö, Julius;
Hundi, Sruthi;
Jokinen, Tarja S.;
Suonto, Emilia;
Teräväinen, Eeva;
Donner, Jonas;
La Rovere, Rita;
Bultynck, Geert;
Ylikallio, Emil;
Tyynismaa, Henna;
Lohi, Hannes

Publication type:

Article

Treatment of teeth in the esthetic zone in a patient with amelogenesis imperfecta using composite veneers and the clear matrix technique: A case report.

Published in:

2016

By:

Bogosavljević, Aleksandar;
Mišina, Vanja;
Jordačević, Jovana;
Abazović, Milka;
Dukić, Smiljka;
Ristić, Ljubiša;
Daković, Dragana

Publication type:

Case Study

Front & Back Matter.

Published in:: Fetal Diagnosis & Therapy, 2013, v. 33, n. 3, p. X, doi. 10.1159/000351806
Publication type:: Article

Amelogenesiz İmperfektalı Erişkin Bir Hastanın Tam Dijital İş Akışı ile Protetik Rehabilitasyonu.

Published in:

Journal of Ege University School of Dentistry / Ege Üniversitesi Dis Hekimligi Fakültesi Dergisi, 2024, v. 45, n. 2, p. 127

By:

DEDE, Doğu Ömür;
POMAY, Mustafa Barış;
ÖNGÖZ DEDE, Figen

Publication type:

Article

Dentinogenesis imperfecta: An update.

Published in:

Journal of Research & Practice on the Musculoskeletal System (JRPMS), 2022, v. 6, n. 1, p. 9, doi. 10.22540/JRPMS-06-009

By:

Tsoukala, Efthimia;
Chochtoula, Georgia;
Theodorou, Iosifina;
Lambrou, George I.

Publication type:

Article

Prosthetic Reconstruction of a Patient with Amelogenesis Imperfecta: A Two-Year Follow-up Evaluation.

Published in:

2025

By:

Geramipanah, Farideh;
Mehrinejad, Parsa;
Yaghoobi, Negin

Publication type:

Case Study

Orthodontic management of amelogenesis imperfecta: A case report.

Published in:

2024

By:

Jha, Kanistika;
Adhikari, Manoj;
Shrestha, Suraksha;
Pandey, Anisha

Publication type:

Case Study

Interdisciplinary full mouth rehabilitation of a patient with amelogenesis imperfecta from childhood to young adult‐hood: A 12‐year case report.

Published in:

2024

By:

Caussin, Élisa;
Courson, Frédéric;
Dursun, Elisabeth;
Brukarz, Yohann;
Dot, Daniel;
Chaussain, Catherine;
Attal, Jean‐Pierre;
François, Philippe

Publication type:

Case Study

Managing vertical dimensions in patients with Amelogenesis Imperfecta: A case report.

Published in:

2022

By:

Farao, Warren;
Roomaney, Imaan A.

Publication type:

Case Study

Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report.

Published in:

Clinical Case Reports, 2022, v. 10, n. 4, p. 1, doi. 10.1002/ccr3.5459

By:

Mascarell, Salomé;
Citterio, Hélène;
Martiano, Victor;
Friedlander, Lisa

Publication type:

Article

Restoration of the dentition in a patient with a history of bruxism and amelogenesis imperfecta: A clinical report.

Published in:

Clinical Case Reports, 2021, v. 9, n. 2, p. 898, doi. 10.1002/ccr3.3667

By:

Tang, Yuyao;
Cao, Tiandong;
Zhang, Ling;
Bao, Guangjie;
Kang, Hong

Publication type:

Article

Amelogenesis imperfecta with Class III malocclusion, reduced crown size and decreased OVD: A multi‐disciplinary management and a 5‐year follow‐up.

Published in:

Clinical Case Reports, 2020, v. 8, n. 8, p. 1440, doi. 10.1002/ccr3.2874

By:

Labidi, Amel;
Bekri, Sana;
Mabrouk, Yosra;
Ben Mustapha, Jouda;
Omezzine, Monia;
Ghoul‐Mazgar, Sonia;
Mansour, Lamia

Publication type:

Article

Rehabilitation of a patient with amelogenesis imperfecta and severe open bite: A multidisciplinary approach.

Published in:

Clinical Case Reports, 2019, v. 7, n. 2, p. 275, doi. 10.1002/ccr3.1966

By:

Arshad, Mahnaz;
Shirani, Gholamreza;
Mahgoli, Hossein‐Ali;
Vaziri, Nastaran

Publication type:

Article

Alternative prosthodontic-based treatment of a patient with hypocalcified type Amelogenesis Imperfecta.

Published in:

Clinical Case Reports, 2017, v. 5, n. 7, p. 1093, doi. 10.1002/ccr3.1005

By:

Jivanescu, Anca;
Miglionico, Antonio;
Barua, Souman;
Hategan, Simona Ioana

Publication type:

Article

Amelogenesis Imperfecta with Taurodontism, Microdontia and Minor Thalassemia: A Case Report.

Published in:

2014

By:

Mazhari, Fatemeh;
Amirmajdi, Negar Mokhtari

Publication type:

Case Study