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1 AHO is caused by heterozygous inactivating mutations in
2 from four crosses (B73 x OH43, Mo17 x A632, AHO x A632, Latente x A632) revealed that alleles of the
5 n different patterns of aqueous angiographic AHO improvement whose further understanding may advance
6 regions of baseline low or high angiographic AHO in each eye (n = 2 eyes with enough space to place t
10 ed equivalent results when comparing another AHO mutation in Galphas (D173N) with a counterpart cance
17 affinity leading to the loss-of-function in AHO whereas Galphao-R243H has a mild decrease in nucleot
23 us, AA demonstrated sustained improvement of AHO for the first time after effective IOP lowering from
24 understanding may advance basic knowledge of AHO and possibly enhance intraocular pressure reduction
26 beculotomy, there was an increased number of AHO branches (p=0.016) and branch junctions (p=0.02).
29 at the same mutation can cause either POH or AHO was observed within a single family, in which the ph
30 ion in Albright's hereditary osteodystrophy (AHO) and a recent report of two patients with AHO who ha
32 esity in Albright hereditary osteodystrophy (AHO) patients, but only when the mutations occur on the
38 is study, we compared aqueous humor outflow (AHO) pathway patterns using aqueous angiography before c
39 to underlie increased aqueous humor outflow (AHO) resistance, which leads to elevated ocular pressure
40 I should be strongly considered after pelvic AHO is detected, and MRI might be substituted diagnostic
42 of the association of abscesses with pelvic AHO, however, the use of MRI should be strongly consider
43 r puncture model, we determined that reduced AHO altered the fate of SC both during development and u
47 tal scintigraphy is the first test used when AHO is suspected but radiographs are negative remains hi
48 present with multihormone resistance and why AHO patients demonstrate resistance to some hormones [e.
51 HO) and a recent report of two patients with AHO who had atypically extensive heterotopic ossificatio