Results 201 to 210 of about 78,624 (321)

Incidence of frontal sinus aplasia in Indian population

, 2016
Sanu P. Moideen, M. Afroze, M. Mohan, M. Regina, R. M. Sheriff, Cini P. Moideen   +5 more
semanticscholar   +1 more source

Genetics of aplasia cutis reveal novel regulators of skin morphogenesis.

Journal of Investigative Dermatology, 2015
Alexander G. Marneros
semanticscholar   +1 more source

Immune-Mediated Multilineage Cytopenias in Thymoma: A Retrospective Case Series. [PDF]

Thorac Cancer
Hu N, Wei Y, Lin W, Dong X, Wang H.
europepmc   +1 more source

Hair Collar Sign with Naevus Flammeus: A Possible Sign of Aplasia Cutis Congenita. [PDF]

Dermatol Pract Concept
Han L, Rao L, Wu YB, Deng YY, Luo B.
europepmc   +1 more source

Atrophic, translucent plaque on the scalp of a newborn. [PDF]

JAAD Case Rep
Bitar RA, Servattalab SE, Damji Y.
europepmc   +1 more source

Acquired pure red cell aplasia associated with malignant lymphomas: A nationwide cohort study in Japan for the PRCA Collaborative Study Group [PDF]

, 2008
Makoto Hirokawa, Kenichi Sawada, Naohito Fujishima, Fumio Kawano, Akiro Kimura, Takashi Watanabe, Ayako Arai, Toshimitsu Matsui, Shinji Nakao, Akio Urabe, Mitsuhiro Omine, Keiya Ozawa   +11 more
openalex   +1 more source

Aplasia medular secundaria a la infección por el virus del dengue

Revista Cubana de Hematología, Inmunología y Hemoterapia
La aplasia medular es una enfermedad hematológica caracterizada por citopenia periférica y una marcada hipocelularidad medular. Esta es una rara complicación de infecciones como la fiebre hemorrágica del dengue.
Francisco Valdés Cabrera, Mildrey Gil Agramonte, Jesús Serrano Mirabal, Andrea Menéndez Veitía, Sergio Machin García, Alejandro González Otero   +5 more
doaj  

FGF10/IGSF3 Variants in Bony Congenital Nasolacrimal Duct Obstruction: A Genotype-Phenotype Study of Syndromic Versus Isolated Disease. [PDF]

Invest Ophthalmol Vis Sci
Li Y, Feng ZX, Cui Y, Sun J, Liu W, Xiao X, Quan X, Zhang C, Li L.   +8 more
europepmc   +1 more source

Concurrent Presentation of Pure Red Cell Aplasia and Myeloproliferative Neoplasm, Unclassifiable With JAK2 and MPL Mutations. [PDF]

Case Rep Hematol
Li Q, Tan L, Wang X, Fan Q.
europepmc   +1 more source

Adams-Oliver syndrome: an unusual congenital disorder. [PDF]

Oxf Med Case Reports
Jarjanazi L, Kebbeh S, Alam E, Saado Q, Jarjanazi M, Alkadi L, Etr A, Aswad TG, Nawfal H.   +8 more
europepmc   +1 more source