Results 41 - 50 for Δ yeotop3.com Δ 여탑 신방화오피◈단단한◈신방화키스방✽신방화오피➣신방화립카페め신방화휴게텔ま신방화스파と신방화출장
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Aphasia | Johns Hopkins Medicine
<b>Aphasia</b> is a language disorder that affects how you communicate. It's caused by damage in the area of the brain that controls language expression and</b> ...
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Salivary Stones | Johns Hopkins Medicine
Request an Appointment. 443-997-6467 Maryland. 855-695-4872 Outside of Maryland. +1-410-502-7683 International. Find a Doctor. <b>Salivary stones</b>, also called</b> ...
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Paroxysmal Supraventricular Tachycardia (PSVT) - Johns Hopkins Medicine
410-955-5000 Maryland. 855-695-4872 Outside of Maryland. +1-410-502-7683 International. <b>Paroxysmal supraventricular tachycardia</b> (PSVT) is a type of abnormal</b> ...
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Spinal Cord Compression | Johns Hopkins Medicine
<b>Spinal cord compression</b> can occur anywhere from your neck (cervical spine) down to your lower back (very top of lumbar spine). Symptoms include numbness,</b> ...
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Salpingectomy | Johns Hopkins Medicine
Salpingectomy is the surgical removal of one or both fallopian tubes. Fallopian tubes are structures that allow eggs to travel from the ovaries to the uterus.</b> ...
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Femoral Popliteal Bypass Surgery | Johns Hopkins Medicine
<b>Femoral popliteal bypass surgery</b> is used to treat a blocked femoral artery. The femoral artery is the largest artery in the thigh. It supplies oxygen-rich</b> ...
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X-Rays | Johns Hopkins Medicine
Request an Appointment. 443-997-7237 Maryland. 855-695-4872 Outside of Maryland. +1-410-502-7683 International. Find a Doctor. Detailed information on x-ray,</b> ...
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Sickle Cell Disease | Johns Hopkins Medicine
<b>Sickle cell disease</b> is an inherited blood disorder marked by defective hemoglobin. It inhibits the ability of hemoglobin in red blood cells to carry oxygen.</b> ...
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Craniofacial Abnormalities | Johns Hopkins Medicine
Craniofacial malformations, including craniosynostosis, are the result of an infant’s skull or facial bones fusing together too soon or in an abnormal way. When</b> ...
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Neurofibromatosis Type 1 (NF1) | Johns Hopkins Medicine
Neurofibromatosis type 1 (NF1) is a condition caused by a change in a specific gene, and therefore can be inherited and passed on. Not all people with NF1 inherit</b> ...
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