Results 151 to 160 of about 37,007 (288)

Facial Annular Lesions in a 28‐Year‐Old Man

JEADV Clinical Practice, EarlyView.
Maximiliano Maass, Angelo Gonzalez, Paula Giacaman, Ester Santander   +3 more
wiley   +1 more source

Acquired narcolepsy secondary to a presumptive hypothalamic hamartoma in a young German wirehaired pointer dog

Veterinary Record Case Reports, EarlyView.
Abstract A 3‐year‐old, male, entire, German wirehaired pointer dog was presented with a 2‐year history of paroxysmal episodes of collapse associated with reduced levels of consciousness. A magnetic resonance imaging study identified a single, ill‐defined, non‐contrast‐enhancing, intra‐axial mass lesion involving the hypothalamus.
Callum Atkins, Tessa V. Procter, Tobias Schwarz, Megan Madden   +3 more
wiley   +1 more source

Diminished bactericidal capacity for group B streptococci of neutrophils from children with chronic granulomatous disease [PDF]

, 1983
J Stroobant, Mary Catherine Harris, Carolyn S. Cody, Richard A. Polin, Steven D. Douglas   +4 more
openalex   +1 more source

Focal myasthenia gravis in a 4‐year‐old Chihuahua cross dog presented for apparent vomiting

Veterinary Record Case Reports, EarlyView.
Abstract A 4‐year‐old, female, neutered Chihuahua cross was presented with a history of chronic apparent vomiting and coughing. Upon further questioning, regurgitation was suspected rather than vomiting. Conscious thoracic radiographs revealed generalised megaoesophagus.
Martyn A. Wray, Robert E. Shiel, Pedro J. Guzmán Ramos   +2 more
wiley   +1 more source

DNA linkage analysis of X chromosome-linked chronic granulomatous disease. [PDF]

, 1986
Robert L. Baehner, Louis M. Kunkel, Anthony P. Monaco, J.L. Haines, P. M. Conneally, Catherine Palmer, Nyla A. Heerema, Stuart H. Orkin   +7 more
openalex   +1 more source

Granulomatous mural folliculitis and cytotoxic interface dermatitis in a pygmy goat associated with ovine herpesvirus‐2 and systemic lesions of malignant catarrhal fever

Veterinary Record Case Reports, EarlyView.
Abstract A 1‐year‐old pygmy goat presented with progressive alopecia, skin ulceration and lichenification over the neck, face and body. Empirical treatment for parasitic and fungal causes of skin disease did not produce clinical improvement, prompting a full diagnostic investigation.
Peter Richards‐Rios, Dominic Sharkey
wiley   +1 more source

Clinical periodontal diagnosis

Periodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi, Andrea Roccuzzo, Jean‐Claude Imber, Alexandra Stähli, Björn Klinge, Niklaus P. Lang   +5 more
wiley   +1 more source

Rasamsonia sp: An emerging infection amongst chronic granulomatous disease patients. A case of disseminated infection by a putatively novel Rasamsonia argillacea species complex involving the heart

Medical Mycology Case Reports, 2019
Chronic granulomatous disease (CGD) is a heterogeneous condition due to defects in NADPH oxidase characterized by granuloma formation and increased susceptibility to invasive infections, in particular moulds.
Ahmed Babiker, Nupur Gupta, Connie F.C. Gibas, Nathan P. Wiederhold, Carmita Sanders, James Mele, Hongxin Fan, Alina Iovleva, Ghady Haidar, Carolyn Fernandes   +9 more
doaj  

Monoclonal antibody 7D5 raised to cytochrome b558 of human neutrophils: immunocytochemical detection of the antigen in peripheral phagocytes of normal subjects, patients with chronic granulomatous disease, and their carrier mothers [PDF]

, 1987
Michio Nakamura, M Murakami, T. Koga, Yuto Tanaka, S Minakami   +4 more
openalex   +1 more source

Sauteur d'Alfort rabbit‐like locomotory disturbances and eye disorders in two pet rabbits—‘handstand rabbits’

Veterinary Record Case Reports, EarlyView.
Abstract Homozygous sauteur d'Alfort rabbits have a splicing‐site mutation in the RAR‐related orphan receptor B (RORB) gene that causes changes in their locomotion. These rabbits sometimes walk on their thoracic limbs, especially at higher speeds. They also experience additional abnormalities, including eye alterations such as blindness due to retinal ...
Kerstin Müller, Sabine Schulze, Katharina Thieme, Robert Klopfleisch, Miguel Carneiro   +4 more
wiley   +1 more source