Results 81 to 90 of about 257,150 (173)

Pelger-Huët anomaly in two related mixed-breed dogs

, 2011
A 6-month-old male mixed-breed dog weighing 12.6 kg weight was presented for evaluation of a subcutaneous nodule on the dorsum. The medical history indicated trimethoprim–sulfamethoxazole treatment 2 months before presentation at the veterinary hospital.
Loreno R. Tomaz, Rejane S. Sousa, Benito Soto-Blanco, André M. Vale   +3 more
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Homozygotic Pelger-Huet\u27s nuclear anomaly of granulocytes in peripheral blood smear (human)

, 2007
Stain: May-Grnwald-Giemsa (MGG). In this case of homozygotic Pelger-Hut anomaly the neutrophil (1) as well as the eosinophil (2) have non-lobed nuclei with condensed chromatin.
Poels, Lambert G.
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Polychromatic Red Blood Cell with Cabot Ring, Normoblast, and Polymorphonuclear Leukocytes

, 2002
Cabot ring in polychromatic RBC, normoblast, & Pelger-Huet ...
Lawrence, Christine
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Homozygotic Pelger-Hut\u27s nuclear anomaly of neutrophilic granulocytes in peripheral blood smear (human)

, 2007
Stain: May-Grnwald-Giemsa (MGG). The neutrophils in this patient with homozygotic Pelger-Hut\u27s anomaly have non-lobed nuclei.
Poels, Lambert G.
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Pelger-Huët anomaly study in a family

, 2008
The Pelger-Huët anomaly is a dominant autosomal disease, characterized by the incomplete segmentation of the granulocytes nucleus without lost of the cellular function.
Calderan, Patrícia H. O., Campiolo, Dimas J., Saavedra, Omar S. G., Bonini-Domingos, Claudia Regina [UNESP]   +3 more
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Peripheral Blood Smear Findings of COVID-19 Patients Provide Information about the Severity of the Disease and the Duration of Hospital Stay

Background: Data about the morphological changes in peripheral blood smears during COVID-19 infection and their clinical severity association are limited.
Aydogdu, I, Bag, HGG, Berber, I, Sarici, A, Cagasar, O, Delen, LA, Berber, NK, Ulutas, O, Yildirim, A   +8 more
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Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly.

, 2003
The nature of the wild-type gene product at the mouse ichthyosis (ic) locus has been of great interest because mutations at this locus cause marked abnormalities in nuclear heterochromatin, similar to those observed in Pelger-Huet anomaly (PHA).
Olins, A L, Hoffmann, K, Burzenski, L M, Olins, D E, Sperling, K, Shultz, L D, Gott, B, Herrmann, H, Schweitzer, P A, Lyons, B L, Dreger, C, Kalscheuer, V, Samuels, R   +12 more
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Hereditary immunological diseases in dogs

, 2015
This thesis summarizes the most important findings of primary immunodeficiencies in different breeds of dogs, their genetic background, symptoms, their treatment options: canine leukocyte adhesion deficiency, trapped neutrophil syndrome, Pelger-Huet ...
KREJČOVÁ, Lenka
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Case of acquired or pseudo-Pelger-Huët anomaly. [PDF]

Oxf Med Case Reports, 2015
Ayan MS, Abdelrahman AA, Khanal N, Elsallabi OS, Birch NC.   +4 more
europepmc   +1 more source

Anomalia de Pelger Huet em cão da raça pastor australiano – relato de caso

          A Anomalia de Pelger Huet (APH) é um distúrbio genético considerado autossômico dominante, responsável pela hipossegmentação dos núcleos dos granulócitos, especialmente dos neutrófilos, devido a uma falha na ...
Salzedas, Breno Aguiar, Silva, Larissa Lins Correia da   +1 more
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