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UnknownClassifying Ectopia Lentis in Marfan Syndrome into Five Grades of Increasing Severity.
Not available
S-EPMC7141252 | biostudies-literature
UnknownObstetrical and neonatal complications in hereditary haemorrhagic telangiectasia: A retrospective study.
Not available
S-EPMC10092409 | biostudies-literature
UnknownAltered expressions of CXCR4 and CD26 on T-helper lymphocytes in hereditary hemorrhagic telangiectasia.
Not available
S-EPMC8670161 | biostudies-literature
UnknownFuture treatments for hereditary hemorrhagic telangiectasia.
Not available
S-EPMC6945546 | biostudies-literature
UnknownHereditary hemorrhagic telangiectasia: from signaling insights to therapeutic advances.
Not available
S-EPMC10866657 | biostudies-literature
UnknownEuropean Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT).
Not available
S-EPMC6094583 | biostudies-literature
UnknownPhenotypic characterisation of SMAD4 variant carriers.
Not available
S-EPMC11287639 | biostudies-literature
UnknownPrevention of serious infections in hereditary hemorrhagic telangiectasia: roles for prophylactic antibiotics, the pulmonary capillaries-but not vaccination.
Not available
S-EPMC6355489 | biostudies-literature
UnknownSequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia.
Not available
S-EPMC7507685 | biostudies-literature
UnknownBEST study: one-year descriptive follow-up of bevacizumab treatment in hereditary haemorrhagic telangiectasia post-BABH interventional study.
Not available
S-EPMC12033602 | biostudies-literature
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