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Browse Familial diseases topic


1-56 out of 56 article(s)
Title Author Type Date Words
A Case of Familial Male-limited Precocious Puberty with a Novel Mutation. Gurnurkar, Shilpa; DiLillo, Emily; Carakushansky, Mauri Clinical report Jun 1, 2021 3090
Outcomes of Dyslipidemia Screening Program in School-aged Children. Kose, Engin; Kose, Melis; Topcu, Sipil; Matur, Busra; Baris, Buket; Ozkan, Behzat Report Jun 1, 2021 4188
The Relationship of Mutation Carriage of BRCA1/2 and Family History in Triple-Negative Breast Cancer: Experience from a Diagnostic Center in Turkey. Duzkale, Neslihan; Kandemir, Olcay Report Apr 1, 2021 4497
Puumala Virus Infection in Family, Switzerland. Vetter, Pauline; LHuillier, Arnaud G.; Montalbano, Maria F.; Pigny, Fiona; Eckerle, Isabella; Torria Clinical report Feb 1, 2021 1415
Lipid-lowering drug class slashes LDL in homozygous familial hypercholesterolemia. Zoler, Mitchel L. Apr 1, 2020 878
GENETIC ANALYSIS OF FAMILIES HAVING AUTOSOMAL RECESSIVE INTELLECTUAL DISABILITY. Khan, Jamshed; Junaid, Muhammad; Uddin, Shahab; Moeed, Khalida; Ullah, Usman; Aman, Shehla Report Jun 30, 2019 2695
You Can Overcome a Family History of Cardiovascular Disease. Mar 1, 2019 732
Myeloid Neoplasm With Germline Predisposition: A 2016 Update for Pathologists. Gao, Juehua; Gong, Shunyou; Chen, Yi-Hua Report Jan 1, 2019 7322
Familial history of hypertension-induced impairment on heart rate variability was not observed in strength-trained subjects. Santa-Rosa, F.A.; Shimojo, G.L.; Sartori, M.; Rocha, A.C.; Francica, J.V.; Paiva, J.; Irigoyen, M.C. Report Dec 1, 2018 3264
Identifying suspected familial chylomicronemia syndrom. Rengarajan, Ronak; McCullough, Peter A.; Chowdhury, Anima; Tecson, Kristen M. Report Jul 1, 2018 3310
Heterozygous HTRA1 missense mutation in CADASIL-like family disease. Wu, Xiaowei; Li, Changxin; Mao, Jinming; Li, Ling; Liu, Yan; Hou, Yao Report May 1, 2018 2838
Phenotypic variability and genetic susceptibility of schizophrenia-evidence from a family study. Crama, Adina; Buzut, Marina; Gaina, Marcel-Alexandru; Chirita, Vasile; Bolos, Alexandra; Chirita, Ro Report Mar 1, 2018 3632
Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East. Abu-Duhier, Faisel; Pooranachandran, Vivetha; McDonagh, Andrew J.G.; Messenger, Andrew G.; Cooper-Kn Clinical report Jan 1, 2018 4276
Bleeding disorders (part 1). Alli, N. Guest commentary Dec 28, 2017 643
Familial Homozygous Hypercholesterolaemia--a case report. Potdar, Shailaja; Panot, Jayesh; Kumavat, Vandana; Junagade, Sunil Clinical report Mar 2, 2017 1689
Mathematical Modeling for Inherited Diseases. Anis, Saima; Khan, Madad; Khan, Saqib Report Jan 1, 2017 4720
Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease. He, Ya-Chao; Huang, Pei; Li, Qiong-Qiong; Sun, Qian; Li, Dun-Hui; Wang, Tian; Shen, Jun-Yi; Du, Juan Report Jan 1, 2017 3328
Risk for depression may be handed down through generations. Brief article Nov 1, 2016 153
Locating legacy in illness. Froude, Cameron Kiely Jun 1, 2016 1603
Is consanguineous marriage responsible for congenital cardiac and extra-cardiac anomalies? Bage, Nutan Nalini; Rao, Sudha Report Mar 7, 2016 2102
The reproductive behavior of families with Thalassemic children in Hormozgan. Moradabadi, Ali Safari; Alavi, Azin; Eftekhaari, Tasnim Eqbal; Dadipoor, Sakineh Report Jul 1, 2015 2407
Familial exudative vitreoretinopathy/Ailevi eksudatif vitreoretinopati. Sizmaz, Selcuk; Yonekawa, Yoshihiro; Trese, Michael T. Report Jul 1, 2015 2952
Multiple minute digitate hyperkeratosis affecting the face and folds: clinical, dermoscopic, and histological report of a familial case. Correia, Osvaldo; Rocha, Natividade; Haneke, Eckart Clinical report Oct 1, 2014 1051
Prevalence of impaired glucose tolerance test in first degree relatives (>30yrs) of type II diabetes mellitus patients: original report. Manjhvar, Shailendra Kumar; Gupta, Hariom; Valame, Shaunak Report Aug 21, 2014 2704
A case report of dominant dystrophic epidermolysis bullosa in siblings: a rare genetic disorder with a therapeutic challenge. Sharma, Harsh; Varma, Krishnendra Clinical report Aug 4, 2014 1175
A case of familial renal glucosuria with hypercalciuria and selective argininuria/Hiperkalsiuri ve selektif argininuri birlikteliginde ailesel bobrek glukozuri olgusu. Turkmen, Aysel Vehapoglu; Nursoy, Mustafa Atilla; Turkmen, Serdar; Yazici, Mehmet Letter to the editor Sep 1, 2013 1162
T.H. Pullar memorial address. Pathology: the study of structure and function in health and diseases. Fraser, Robin Report Nov 1, 2012 2713
Familial facial palsy/Ailevi yuz felci. Ekici, Baris; Tatli, Burak; Uzmen, Meral Report Mar 1, 2012 938
Siblings of those with leg blood clots face higher clot risks. Brief article Oct 1, 2011 147
Shame shift: placing the blame. Brief article Jan 1, 2011 251
Family genomics makes its debut: full DNA studies of parents and children pinpoint mutations. Sanders, Laura Apr 10, 2010 460
Know your family's health history for a better future. Johnson, Teddi Dineley Dec 1, 2008 786
Toddlers and hypercholesterolemia. Brief article Nov 15, 2007 237
Rare periodic fever syndromes erupt on skin. Splete, Heidi Clinical report Oct 1, 2007 1081
Limited family structure and BRCA gene mutation status in single cases of breast cancer. Barrett-Lee, Peter Clinical report Sep 1, 2007 307
Shaking off the shadow of ovarian cancer. Klebanow, Diana Jul 1, 2007 1991
BP screen for stroke offspring warranted. Wendling, Patrice Clinical report Feb 1, 2007 343
Familial trend detected in Barrett's esophagus. Dixon, Bruce K. Aug 1, 2006 529
Genetic and transmission analysis of Helicobacter pylori strains within a family (1). Dauga, Catherine Oct 1, 2004 4039
Signs of autism present as early as 6 months: first longitudinal study of high-risk sibs. Walsh, Nancy Aug 1, 2003 447
Tonsil with Tangier disease. (Pathology Clinic). Thompson, Lester D.R. Brief Article Mar 1, 2003 265
Increased prevalence of malignant diseases in the close neighborhood of children with cancer. (Features). Ludvigsson, Johnny Statistical Data Included Mar 1, 2002 3615
Twin Study of ADHD. (Clinical Capsules). Splete, Heidi Jan 1, 2002 133
Don't Overlook Catatonic Schizophrenia Diagnosis. (More Cases Than Previously Imagined). Sherman, Carl Nov 1, 2001 260
Surveying the genetic roots of cancer. Oct 1, 2001 196
Low-Dose Insulin Fails to Stave Off Diabetes Risk. TUCKER, MIRIAM E. Aug 1, 2001 472
Spouses Are Likely to Share the Same Chronic Diseases. JANCIN, BRUCE Jul 15, 2001 281
Approach to the Diagnosis of Thin Basement Membrane Nephropathy in Females With the Use of Antibodies to Type IV Collagen. Lajoie, Ginette May 1, 2001 3852
Hereditary Cancer Syndromes. Frank, Thomas S. Jan 1, 2001 5533
ADD/ADHD All in the Family. Spivey, J. Carlisle Dec 1, 2000 2090
Sorting Out Inherited Colorectal Cancer Syndromes. WORCESTER, SHARON Brief Article Apr 15, 2000 603
Early Menopause Appears to Have Familial Connection. JOHNSON, KATE Dec 1, 1999 386
Familial Multiple Endocrine Neoplasia Type 1. Pamphlet Jun 1, 1997 3325
Tracing your family's medical tree. Sep 1, 1991 1649
The genetics of cancer. Mulvihill, John J. Pamphlet May 1, 1990 2886
Schizophrenia gene: a family link fades. Bower, B. Jun 10, 1989 326

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