Results 131 to 140 of about 10,204 (285)

The clinical meaning of histamine skin reactivity [PDF]

open access: yes, 2015
The definition of the “atopic state”, i.e. subjects presenting at least one skin wheal with a minimum diameter of 3 mm induced by an allergen skin-prick test (ASPT), is based on the assumption that wheal size depends entirely on the amount of histamine
BARRETO, Mario, RONCHETTI, ROBERTO
core   +1 more source

Acromegaly, Herniation of Cerebellar Tonsils, and Arnold–Chiari 1 Malformation: The Importance of Right Definitions

open access: yesCase Reports in Endocrinology, Volume 2024, Issue 1, 2024.
We present a case of acromegaly associated with Arnold–Chiari 1 malformation and a literature review regarding this association, mainly focusing on the importance of a clear distinction between Chiari malformation and herniation of cerebellar tonsils (CTH).
Alessandro Ciarloni   +2 more
wiley   +1 more source

Allergic manifestations and cutaneous histamine responses in patients with McCune Albright syndrome

open access: yesWorld Allergy Organization Journal, 2013
Background McCune Albright syndrome (MAS) is a rare disorder characterized by precocious puberty, café-au-lait spots, and fibrous dysplasia. Its cause is an activating mutation in the GNAS gene, encoding a subunit of the stimulatory G protein, Gsalpha ...
Jill D Jacobson   +2 more
doaj  

McCune Albright syndrome: A case report with review of literature

open access: yesJournal of Orthopedics, Traumatology and Rehabilitation, 2014
McCune Albright syndrome (MAS) is a rare disorder comprising any two of polyostotic fibrous dysplasia (PFD), café-au-lait macules and endocrine abnormalities. We present the case of a 25-year-old male who suffered a pathologic fracture of his right femur
Muhammad Haseeb   +3 more
doaj   +1 more source

Familial Micronodular Adrenocortical Disease, Cushing Syndrome, and Mutations of the Gene Encoding Phosphodiesterase 11A4 ( PDE11A) [PDF]

open access: yes, 2014
We present the pathologic findings in the adrenal glands of 4 patients, aged 10 to 38 years, with Cushing syndrome and germline inactivating mutations of the gene PDE11A4 that encodes phosphodiesterase11A4. The gene is expressed in the adrenal cortex and
Bertherat, J.   +3 more
core   +1 more source

Correction of Data and Syndrome Errors by Stabilizer Codes [PDF]

open access: yesarXiv, 2016
Performing active quantum error correction to protect fragile quantum states highly depends on the correctness of error information--error syndromes. To obtain reliable error syndromes using imperfect physical circuits, we propose the idea of quantum data-syndrome (DS) codes that are capable of correcting both data qubits and syndrome bits errors.
arxiv  

Learning from the Syndrome [PDF]

open access: yesarXiv, 2018
In this paper, we introduce the syndrome loss, an alternative loss function for neural error-correcting decoders based on a relaxation of the syndrome. The syndrome loss penalizes the decoder for producing outputs that do not correspond to valid codewords.
arxiv  

A non-classic form of McCune Albright syndrome with different presentations and review of the literatures

open access: yesCaspian Journal of Internal Medicine, 2021
Background: McCune Albright syndrome (MAS) is a rare heterogeneous clinical syndrome without any predilection for ethnic group.  Classic form includes triad of fibrous dysplasia, café au late spots and autonomous hyper function of one or more endocrine ...
Ali Reza Navabazam   +3 more
doaj  

The Role of gsp Mutations on the Development of Adrenal Cortical Tumors and Adrenal Hyperplasias

open access: yesFrontiers in Endocrinology, 2016
Somatic GNAS point mutations, commonly known as gsp mutations, are involved in the pathogenesis of McCune Albright syndrome and have also been described in autonomous hormone-producing tumors, such as somatotropinoma, corticotrophoma, thyroid cancer ...
Maria Candida Barisson Villares Fragoso   +3 more
doaj   +1 more source

Dental Perspectives in Fibrous Dysplasia and McCune-Albright Syndrome [PDF]

open access: yes, 2013
McCune-Albright syndrome (MAS) is a rare multisystem disorder characterized by the triad of polyostotic fibrous dysplasia (PFD), endocrine disorders and café-au-lait skin pigmentation.
Akintoye, Sunday O   +2 more
core   +2 more sources

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