Results 111 to 120 of about 3,771 (192)

When teeth and kidneys fail together: a case series of amelogenesis imperfecta-renal syndromes in childhood. [PDF]

Pan Afr Med J
Nouir S, Boukadida R, Hannachi S, Harbi A, Mokni H, Ajmi H, Mabrouk S.   +6 more
europepmc   +1 more source

Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification. [PDF]

Front Physiol, 2023
Bloch-Zupan A, Rey T, Jimenez-Armijo A, Kawczynski M, Kharouf N, O-Rare consortium, Dure-Molla M, Noirrit E, Hernandez M, Joseph-Beaudin C, Lopez S, Tardieu C, Thivichon-Prince B, ERN Cranio Consortium, Dostalova T, Macek M, International Consortium, Alloussi ME, Qebibo L, Morkmued S, Pungchanchaikul P, Orellana BU, Manière MC, Gérard B, Bugueno IM, Laugel-Haushalter V.   +25 more
europepmc   +1 more source

Understanding the Real Needs and Expectations of French Patients with Amelogenesis Imperfecta Through Facebook Content: A Qualitative Thematic Analysis. [PDF]

Healthcare (Basel)
Mailloux A, Dinet J, Filloux J, Lanuel Y.   +3 more
europepmc   +1 more source

Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta. [PDF]

J Pers Med, 2023
Kim YJ, Zhang H, Lee Y, Seymen F, Koruyucu M, Kasimoglu Y, Simmer JP, Hu JC, Kim JW.   +8 more
europepmc   +1 more source

Multidisciplinary management of skeletal and dental vertical dimensions of patients with Amelogenesis Imperfecta isolated type

, 2018
Fanny Henry
openalex   +1 more source

[Amelogenesis imperfecta].

Istanbul Universitesi Dishekimligi Fakultesi dergisi = The journal of the Dental Faculty of Istanbul, 1971
R, Luberti, G, Moize
openaire   +3 more sources

Integrating Imaging and Genomics in Amelogenesis Imperfecta: A Novel Diagnostic Approach. [PDF]

Genes (Basel)
Leban T, Fidler A, Trebušak Podkrajšek K, Pavlič A, Tesovnik T, Jenko Bizjan B, Vrhovšek B, Šket R, Kovač J.   +8 more
europepmc   +1 more source

Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta. [PDF]

Eur J Hum Genet, 2023
Resende KKM, Riou MC, Yamaguti PM, Fournier B, Rondeau S, Pacot L, Berdal A, Felizardo R, Mazzeu JF, Cormier-Daire V, Gaucher C, Acevedo AC, de La Dure-Molla M.   +12 more
europepmc   +1 more source

Kohlschütter-Tönz Syndrome: A Rare Clinical Entity with Amelogenesis Imperfecta in Two Siblings, Dental Management and Scoping Review. [PDF]

Turk Arch Pediatr
Şivet EA, Akbeyaz İH, Berkel G, Yeşilyurt A, Sezer B, Menteş A.   +5 more
europepmc   +1 more source

Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion. [PDF]

Intractable Rare Dis Res, 2023
Leite LDR, Resende KKM, Rosa LDS, Mazzeu JF, de Oliveira LC, Scher MDCSD, Acevedo AC, Yamaguti PM.   +7 more
europepmc   +1 more source