Results 111 to 120 of about 88,811 (347)

The Biochemical Profile of Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism during Pregnancy and Lactation: Two Case Reports and Review of the Literature

open access: yesCase Reports in Endocrinology, 2016
Background. Primary hyperparathyroidism (PHPT) and Familial Hypocalciuric Hypercalcemia (FHH) result in different maternal and fetal complications in pregnancy.
Sharmin Ghaznavi, N. Saad, L. Donovan
semanticscholar   +1 more source

Use of Data Mining in the Establishment of Reference Intervals for Albumin‐Adjusted Calcium

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Background Calcium homeostasis is critical for numerous physiological functions, and while total calcium is commonly measured in clinical practice, albumin‐adjusted calcium is widely used to account for protein binding, despite concerns about its accuracy and lack of standardized reference intervals.
Esra Paydaş Hataysal   +1 more
wiley   +1 more source

Status epilepticus secondary to milk-alkali syndrome induced by hypercalcemia (oral antacids) [PDF]

open access: yes, 2011
Milk-alkali syndrome is mainly caused by the ingestion of large amounts of calcium and absorbable alkali. This syndrome can lead to metastatic calcification, renal failure and metabolic alkalosis secondary to hypercalcemia.
Al Samara, Mershed   +2 more
core   +1 more source

Immobilization induced hypercalcemia.

open access: yesCLINICAL CASES IN MINERAL AND BONE METABOLISM, 2016
Immobilization hypercalcemia is an uncommon diagnosis associated with increased bone remodeling disorders and conditions associated with limited movement such as medullar lesions or vascular events.
E. Cano-Torres   +3 more
semanticscholar   +1 more source

PIK3C2A‐Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia Defect

open access: yesClinical Genetics, EarlyView.
Trio exome sequencing allowed the identification of two novel compound heterozygous variants in PIK3C2A, defining the fifth family presenting a PIK3C2A‐related syndrome characterized by pulverulent cataracts and deafness. Functional testing revealed impaired PI metabolism and primary dysfunction phenotype.
Adella Karam   +9 more
wiley   +1 more source

Hypercalcemia. Pathophysiological aspects.

open access: yesPhysiological Research, 2016
The metabolic pathways that contribute to maintain serum calcium concentration in narrow physiological range include the bone remodeling process, intestinal absorption and renal tubule resorption.
I. Z̆ofková
semanticscholar   +1 more source

Medication‐Related Osteonecrosis of the Jaws in Patients on Antiresorptive Medication With Dental Implants. A Scoping Review

open access: yesClinical Oral Implants Research, EarlyView.
ABSTRACT Objectives Patients receiving antiresorptive medication (AR) for osteoporosis or cancer are at risk of medication‐related osteonecrosis of the jaws (MRONJ), especially after surgical procedures. Dental implant (DI) placement in high‐dose AR (HDAR) patients is widely discouraged, and thorough counseling is recommended for low‐dose AR (LDAR ...
Sanne Werner Moeller Andersen   +4 more
wiley   +1 more source

Performance of the pro-FHH score in a delayed diagnosis of familial hypocalciuric hypercalcemia type-1

open access: yesJournal of Clinical and Translational Endocrinology Case Reports, 2021
We present a case of a 50-year-old woman with familial hypocalciuric hypercalcemia type 1 (FHH-1) that was missed during an initial evaluation of hypercalcemia in the setting of normal serum parathyroid hormone (PTH), leading to unnecessary ...
Akuffo Quarde   +2 more
doaj  

Hypercalcemia of Malignancy and Colorectal Cancer

open access: yesWorld Journal of Oncology, 2016
Our aim is to describe the association between colorectal cancer (CRC) and humoral hypercalcemia of malignancy (HHM). Causes of hypercalcemia of malignancy include parathyroid hormone-related peptide (PTHrP) secretion, local osteolysis, calcitriol ...
Rodolfo J. Galindo   +4 more
semanticscholar   +1 more source

Deep developmental phenotyping in children with tuberous sclerosis complex, with and without autism

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16312 Abstract Aim To characterize autism and co‐occurring tuberous sclerosis‐associated neuropsychiatric disorders (TAND) in children with tuberous sclerosis complex (TSC), addressing evidence gaps by using deep developmental phenotyping in a single cohort.
Rebecca A. Mitchell   +4 more
wiley   +1 more source

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