Find link

language:

Find link is a tool written by Edward Betts.

Longer titles found: Renal osteodystrophy (view), Albright's hereditary osteodystrophy (view), Hypertrophic osteodystrophy (view)

searching for Osteodystrophy 26 found (83 total)

alternate case: osteodystrophy

Hypertrophic osteoarthropathy (449 words) [view diff] no match in snippet view article find links to article

Hypertrophic osteoarthropathy is a medical condition combining clubbing and periostitis of the small hand joints, especially the distal interphalangeal

DOOR syndrome (405 words) [view diff] exact match in snippet view article find links to article

DOOR (deafness, onychodystrophy, osteodystrophy, and mental retardation) syndrome is a genetic disease which is inherited in an autosomal recessive fashion

Pseudofracture (150 words) [view diff] exact match in snippet view article find links to article

rarely occurs in Paget's disease of bone, hyperparathyroidism, renal osteodystrophy, osteogenesis imperfecta, fibrous dysplasia, and hypophosphatasia. Looser

Septic arthritis (4,544 words) [view diff] exact match in snippet view article find links to article

general, children and adolescents with hematologic disorders, renal osteodystrophy, and immune-compromised status. In adults, vulnerable groups include

Osteoma (210 words) [view diff] exact match in snippet view article find links to article

as proptosis). Osteoma cutis (also known as "Albright's hereditary osteodystrophy") Osteoid osteoma Fibro-osteoma Chondro-osteoma Osteoma of the frontal

2q37 monosomy (352 words) [view diff] exact match in snippet view article find links to article

delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype". Clin Genet. 66 (6): 537–44. doi:10.1111/j.1399-0004

Archibald's sign (192 words) [view diff] exact match in snippet view article find links to article

commonly found in pseudohypoparathyroidism of Albright's hereditary osteodystrophy, brachydactyly, acrodysostosis, and occasionally with homocystinuria

GPR35 (1,134 words) [view diff] exact match in snippet view article find links to article

delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype". Clin. Genet. 66 (6): 537–44. doi:10.1111/j.1399-0004

Metabolic acidosis (3,835 words) [view diff] exact match in snippet view article find links to article

bone density, resulting in an increased risk of bone fractures, renal osteodystrophy, and bone disease; as well, increased protein catabolism leads to muscle

Panosteitis (726 words) [view diff] exact match in snippet view article find links to article

possible causes of lameness have been ruled out, such as hypertrophic osteodystrophy and osteochondrosis dissecans. History, signalment, and clinical signs

GNAS complex locus (1,688 words) [view diff] exact match in snippet view article find links to article

Mutations in GNAS products are associated with: Albright hereditary osteodystrophy pseudohypoparathyroidism type Ia and Ib pseudopseudohypoparathyroidism

2q37 deletion syndrome (603 words) [view diff] exact match in snippet view article find links to article

Brachydactyly-intellectual disability syndrome, Albright hereditary osteodystrophy type 3 2q37 deletion syndrome is inherited in an autosomal dominant

Who's Driving Doug (459 words) [view diff] exact match in snippet view article find links to article

Doug, an emotional coming-of-age story about a college student with osteodystrophy, is one of those movies that stacks the decks against critical viewers

Fetuin-B (544 words) [view diff] exact match in snippet view article find links to article

PMID 16335952. Coen G, Ballanti P, Balducci A, et al. (2006). "Renal osteodystrophy: alpha-Heremans Schmid glycoprotein/fetuin-A, matrix GLA protein serum

Vitamin and mineral management for dialysis (597 words) [view diff] exact match in snippet view article find links to article

containing phosphorus and potassium. Lack of calcium can lead to renal osteodystrophy (bone weakening). On the other hand, too much calcium can cause calcification

List of eponymous diseases (6,446 words) [view diff] exact match in snippet view article find links to article

Heinrich Albers-Schönberg Albright disease (aka Albright hereditary osteodystrophy, Albright syndrome, McCune–Albight syndrome) – Fuller Albright

List of mammoth specimens (1,370 words) [view diff] exact match in snippet view article find links to article

2017. Strong evidence for dietary mineral imbalance as the cause of osteodystrophy in Late Glacial woolly mammoths at the Berelyokh site (Northern Yakutia

Primary sclerosing cholangitis (3,993 words) [view diff] exact match in snippet view article find links to article

gallbladder due to the high risk of cholangiocarcinoma. Osteoporosis (hepatic osteodystrophy) and hypothyroidism are also associated with PSC.[citation needed] A

Bone morphogenetic protein 7 (2,565 words) [view diff] exact match in snippet view article find links to article

KA (April 2002). "Treatment of a murine model of high-turnover renal osteodystrophy by exogenous BMP-7". Kidney International. 61 (4): 1322–31. doi:10.1046/j

Agalychnis lemur (2,253 words) [view diff] exact match in snippet view article find links to article

lemur leaf frog at EVACC was through poor nutritional condition and osteodystrophy, with a very small number contracting lungworm infection and squamous

Anna-Maria Borissova (375 words) [view diff] exact match in snippet view article find links to article

Dnevnik (in Bulgarian). Retrieved 2023-09-28. "Diabetoporosis or Diabetic Osteodystrophy | Българско дружество по ендокринология". Retrieved 2023-09-28. "Здравният

Genomic Medicine Institute (1,061 words) [view diff] exact match in snippet view article find links to article

disorders inherited cardiovascular pulmonary diseases Albright hereditary osteodystrophy and pseudohypoparathyroidism heart defects neuromuscular disorders autism

Foldex cat (1,170 words) [view diff] exact match in snippet view article find links to article

to health conditions found in the Scottish Fold, such as congenital osteodystrophy, bone abnormalities, and respiratory issues. the average lifespan of

KIF1A (5,565 words) [view diff] exact match in snippet view article find links to article

(2001). "Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR"

Vulture restaurant (2,279 words) [view diff] exact match in snippet view article find links to article

Plug3, I. (1986). "Bone crushing carnivores and their significance to osteodystrophy in griffon vulture chicks". Journal of Zoology. 210 (1): 23–43. doi:10

PET for bone imaging (5,262 words) [view diff] exact match in snippet view article find links to article

measured with positron emission tomography and [18F]fluoride ion in renal osteodystrophy: correlation with bone histomorphometry". Journal of Clinical Endocrinology