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Diagnosis subtopic


1-31 out of 31 article(s)
Title Author Type Date Words
Bardet Biedl syndrome: A rare genetic disorder. Khan, Shahzad Alam; Ansari, Muhammad Zubair Ahmad; Khalid, Muhammad Clinical report Sep 18, 2020 1433
Kimura's disease: a rare disease with cervical lymphadenopathy. Durak, Vahide Aslihan Clinical report Sep 18, 2020 986
A girl presents with orange-red scaly papules and plaques on the trunk, arms, knees. Tracy, Alexis; Eichenfield, Lawrence F. Clinical report Jun 1, 2020 802
Prenatal detection of Peters plus-like syndrome/Peters-plus benzeri sendromun prenatal tanisi. Canda, Mehmet Tunc; Caglayan, Latife Doganay; Demir, Ayse Banu; Demir, Namik Clinical report Dec 1, 2018 1464
Leiomyomatosis peritonealis disseminata in a nonpregnant woman/Nulligravid olguda leiomyomatosis peritonealis disseminata. Aydin, Abdullah; Soylemez, Tuce; Karateke, Ates; Polat, Mesut; Girgin, Burcin Rabia Clinical report Dec 1, 2018 914
Rhinoscleroma. Umphress, Brandon; Raparia, Kirtee Report Dec 1, 2018 3249
Mesentery root: a rare location of Castleman's disease. Anitei, Gabriela Maria; Ioanid, Nicolae Serban; Patrascu, Ana Maria; Cretu, Gica Ciprian; Scripcariu Clinical report Dec 1, 2018 1785
Bilateral Inflammatory Pseudotumour of the Breast: A Case Report and Review of the Literature. Dani, Mohsin; Pinder, Sarah; Fentiman, Ian Clinical report Oct 1, 2018 2386
The Articulating Neural Arch A Rare Developmental Anomaly. Mann, Robert W.; Burch, Ashley; Barnes, Ethne; Teegen, Wolf-Rudiger; Chrysostomou, Popi Th. Report Jun 22, 2018 3676
Progressive Pseudorheumatoid Condrodysplasia, an Unusual Cause of Joint Swelling and Stiffness. Kilic, Esra Report Jun 1, 2018 1048
THE NEXT DAY: STEPS TO TAKE AFTER RECEIVING A DIAGNOSIS: The day after getting a new diagnosis is the first day of your new reality and your family's new lifestyle. You are not alone. You have support and resources available to you. Ostrea, Carrie; Bruns, Anne Cover story Jan 1, 2018 1177
Beyond Urticaria: Schnitzler Syndrome. Ruiz-Villaverde, Ricardo; Bueno-Rodriguez, Ahinoa; Sanchez-Cano, Daniel Case study Sep 1, 2017 717
Rare Location for Dysembryoplastic Neuroepithelial Tumor in the Septum Pellucidum. Dossani, Rimal H.; Patra, Devi; Adeeb, Nimer; Wild, Elizabeth; Ghildyal, Abhilasha; Fowler, Marjorie Clinical report Sep 1, 2017 2695
Characteristics of Good's Syndrome in China: A Systematic Review. Dong, Jin-Pei; Gao, Wen; Teng, Gui-Gen; Tian, Yu; Wang, Hua-Hong Report Jul 5, 2017 4030
Seeing beyond the diagnosis. Waller, Courtney Organization overview Nov 1, 2016 1695
Scarabiasis in children: a prospective study of 6 cases. Mohammed, M.T.P.; Sudhakaran, K.; Venugopalan, A.K. Report May 9, 2016 1243
HAMULAR BURSITIS: DIFFICULT TO DIAGNOSE IN OROFACIAL PAIN. Arya, Sugandha; Singhal, Priya; Vengal, Manoj; Patil, Neelkant; Bhateja, Sumit Report Mar 31, 2015 2633
We want you! A gathering of newborn screening advocates. Raccosta, Maryann Conference notes Sep 1, 2014 777
Kimura disease--a rare case. Pastapur, Rajeev; Ansari, Ashfaque; Bohra, R.B.; Vare, Reena; Mathew, Suma Moni Clinical report Nov 11, 2013 1287
Perforation of jejunal ulcer. Mankar, Kishore K. Clinical report Nov 4, 2013 471
Jeune syndrome. Ramya, H.S.; Shivswamy, Sushanth; Manjunath M.N. Clinical report Jun 1, 2013 1074
Bilateral primary non-Hodgkin's lymphoma of breast. A rare entity. Das, Narayan Clinical report Apr 29, 2013 677
Pyles metaphyseal dysplasia with megalocornea a very rare association--a case report. Mandal, Prasanta Kumar; Majhi, Fagu Ram; Mandal, Anup Clinical report Apr 29, 2013 602
Inflammatory myofibroblastic tumour of the bladder: Case report and review of the literature. Wei, Li; Jianbo, Liang; Qiang, Wei; Hai, Yu; Zhixiang, Lan Report Apr 1, 2013 2196
A case of congenital syndromic hydrocephalus: a subtype of 'Game-Friedman-Paradice syndrome'. Jana, Tapan Kumar; Roy, Hironmoy; Giri, Susmita Jan 1, 2013 1774
The mysterious foreign accent: while treating Ms. D for a suspected psychotic disorder, you learn she has developed a foreign accent. What could be the cause of this unusual symptom? Paul, Panchajanya; Beckman, Barry; Bellian, David; Osinowo, Thomas Report Mar 1, 2011 2169
Rare diseases: where to go for info. Feero, Greg Jan 1, 2009 832
A parent's view of Ohdo syndrome. FitzZaland, Richard; FitzZaland, Mary Clinical report Aug 1, 2008 1262
22q11 deletion syndrome: a mystery no more. Umlauf, Mary Clinical report Aug 1, 2008 2430
Screening and caring for children with rare disorders. Lin, Bruce K.; Fleischman, Alan R. May 1, 2008 685

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