Results 101 to 110 of about 73,460 (305)

Calcinosis Cutis with Large Extension and Uncommon Location in a Dog [PDF]

, 2021
Reiner Silveira de Moraes, Alana Flávia Romani, Andréia Vítor Couto do Amaral, Didier Quevedo Cagnini, Leuton Scharles Bonfim, Mariana Moreira Andraschko   +5 more
openalex   +1 more source

Idiopathic Calcinosis Cutis of the Hand

Plastic and Reconstructive Surgery, Global Open
Summary:. Calcinosis cutis is a disease process characterized by calcified lesions in the skin. Although there are five subtypes of calcinosis, idiopathic calcinosis cutis is a rare disease process with no clear etiology.
Shawhin R.K. Shahriari, MD, Tharani Murali, BS, Tegan N. Clarke, BA, Joseph F. Kuhn, MD, Shelly A. Stepenaskie, MD, Gregory L. Borah, MD, DMD   +5 more
doaj   +1 more source

Successful Treatment of Refractory Sweet's Syndrome With Adalimumab in a Myelodysplastic Syndrome Patient [PDF]

EJHaem
ABSTRACT We report a 69‐year‐old man diagnosed as myelodysplastic syndrome and administrated with azacitidine and selinexor treatment. Then he was revealed high fever and multiple tender erythematous papules involving his mouth, back, upper and lower extremities, which were diagnosed as Sweet's syndrome by skin biopsy.
Ma L, Shen Y, Chang J, Suo S, Wang L, Zhu W, Qiao J, Tong H.   +7 more
europepmc   +2 more sources

Fully Integrated Biochip Platforms for Advanced Healthcare [PDF]

, 2012
Recent advances in microelectronics and biosensors are enabling developments of innovative biochips for advanced healthcare by providing fully integrated platforms for continuous monitoring of a large set of human disease biomarkers.
Baj-Rossi, Camilla, Burleson, Wayne, Carrara, Sandro, Cavallini, Andrea, de Beeck, Maaike Op, Dehollain, Catherine, Ghoreishizadeh, Sara, Guiseppi-Elie, Anthony, Micheli, Giovanni De, Moussy, Francis Gabriel, Olivo, Jacopo, Taurino, Irene   +11 more
core   +5 more sources

Prenatal Identification of a Novel ITGB4 Gene Mutation Associated With Junctional Epidermolysis Bullosa: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
Ultrasonographic characteristics of fetal junctional epidermolysis bullosa associated with ITGB4 gene mutation. ABSTRACT Homozygous or compound heterozygous mutations in the ITGB4 gene are associated with the pathogenesis of junctional epidermolysis bullosa, characterized by increased fragility of the skin and mucous membranes.
Qi Xu, Xiaofang Peng, Wenwen Ma, Xiaoqin Xiao, Liqiong Zhu, Na Di, Xiaojuan Li, Yinglin Liu   +7 more
wiley   +1 more source

Tuberculosis cutis miliaris disseminata as a manifestation of miliary tuberculosis : literature review and report of a case of recurrent skin lesions [PDF]

, 1991
Contains fulltext : 4540.pdf (publisher's version ) (Open ...
Dahlmans, R.P.M., Frantzen, P.J., Koopman, R.J.J., Meer, J.W.M. van der, Rietbroek, R.C., Smedts, F.   +5 more
core   +1 more source

Asproinocybe pakistanica sp. nov. and A. daleyae.: first representatives of the genus Asproinocybe from Pakistan

Nordic Journal of Botany, Volume 2026, Issue 1, January 2026.
Asproinocybe paksitanica sp. nov. is described as a novel species and Asproinocybe daleyae as a new country record from moist temperate forest in Pakistan, based on morphological and molecular data. Morphologically the new species is characterized by a pileus with variable shades from light to chocolate brown, violet lamellae, light brown stipe (light ...
Muhammad Ali, Abdul Rehman Niazi, Urooj Ashraf, Alishba Anam, Najam‐ul‐Sehar Afshan, Mary Catherine Aime, Abdul Nasir Khalid   +6 more
wiley   +1 more source

Cuti sensibili, cuti reattive

EMC - Cosmetologia Medica e Medicina degli Inestetismi Cutanei, 2010
La sindrome «cute sensibile-cute reattiva» e sempre piu comune in tutti i paesi occidentali. Benche i meccanismi di iperreattivita cutanea permettano a poco a poco di spiegarla meglio, i segni clinici restano tuttavia difficili da trattare. Essi non interessano solo il viso, ma possono raggiungere altre localizzazioni, specialmente le mani, i piedi e ...
openaire   +1 more source

Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica

International Journal of Molecular Sciences, 2017
Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance.
A. Kariminejad, F. Afroozan, B. Bozorgmehr, A. Ghanadan, S. Akbaroghli, H. K. Khorram Khorshid, F. Mojahedi, A. Setoodeh, A. Loh, Yu Tan, N. Escande-Beillard, F. Malfait, B. Reversade, T. Gardeitchik, E. Morava   +14 more
semanticscholar   +1 more source

Acute lymphoblastic B‐cell leukemia or CAR‐T cell related skin changes – a relevant diagnostic challenge

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Farzan Solimani, Amrei Dilling, Konrad Heisterkamp, Frederik Damm, Olaf Penack, Christian Oberender, Philipp Le‐Coutre, Martina Rudelius, Kamran Ghoreschi, Alexander Nast   +9 more
wiley   +1 more source