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1-114 out of 114 article(s)
Title Author Type Date Words
Congenital Mucocele of the Nasal Dorsum: A Case Report. Dal, Secil Bahar; Unal, Omer Faruk Clinical report Mar 1, 2021 1186
Congenital heart disease in Africa threatens Sustainable Development Goals. Rossouw, B. Mar 1, 2021 1515
A Male Infant with Congenital Chylous Ascites Accompanied by Hypertension. Altay, Derya; Dursun, Ismail; Gunduz, Zubeyde; Arslan, Duran Clinical report Dec 1, 2020 1711
Congenital Malformations in a Holstein-Fresian Calf with a Unique Mosaic Karyotype: A Case Report. Uzar, Tomasz; Szczerbal, Izabela; Serwanska-Leja, Katarzyna; Gogulski, Maciej; Bugaj, Szymon; Switon Clinical report Sep 1, 2020 3320
Laser-Assisted Endoscopic Cricotracheal Stenosis Resection (CTSR) in Paediatric Congenital Cartilaginous Subglottic Stenosis. Alshammari, Jaber; Arafat, Abdullah; Halawani, Mohammed Jul 31, 2020 3631
The effect of ankaferd blood stopper used for massive haemoptysis in a patient with mounier-kuhn syndrome: A case report. Yazici, Onur; Gulen, Sule Tas; Ceylan, Emel Clinical report Apr 30, 2020 1832
Genetic mapping of autosomal recessive microspherophakia to chromosome 14q24.3 in a consanguineous Pakistani family and screening of exon 36 of LTBP2 gene. Shahzadi, Misbah; Firasat, Sabika; Kaul, Haiba; Afshan, Kiran; Afzal, Rabia; Naz, Shagufta Clinical report Mar 31, 2020 2118
Anomalous origin of the left coronary artery from the pulmonary artery: A surgical certainty. Butt, Ayesha; Amanullah, Muhammad Muneer; Ahmed, Mehnaz Atiq; Hasan, Asif; Ahmad, Waris Clinical report Mar 31, 2020 1856
A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic Polyneuropathy. Oswiecimska, Joanna; Dawidziuk, Mateusz; Gambin, Tomasz; Ziora, Katarzyna; Marek, Marta; Rzonca, Syl Clinical report Sep 1, 2019 4480
Nutritional intervention in berardinelli syndrome or generalized congenital lipoatrophy: case report/INTERVENCAO NUTRICIONAL NA SINDROME DE BERARDINELLI OU LIPODISTROFIA CONGENITA GENERALIZADA: RELATO DE CASO. de Araujo, Edna Karol Rodrigues; Braga, Ana Vaeline Patricio; Tavares, Helder Cardoso; Santana, Mila May 1, 2019 2501
A Novel De Novo Missense Mutation in HNF4A Resulting in Sulfonylurea-Responsive Maturity-onset Diabetes of the Young. Acar, Sezer; Abaci, Ayhan; Demir, Korcan; Ozdemir, Taha Resid; Ozyilmaz, Berk; Bober, Ece Clinical report Sep 1, 2018 2332
ECTODERMAL DYSPLASIA- A CASE OF X-LINKED RECESSIVE DISORDER. Kashid, Avinash Laxmanrao; Patil, Atulkumar Ashokrao Clinical report Mar 26, 2018 2482
Nasu Hakola Disease: A Rare Cause of Dementia and Cystic Bone Lesions, Report of a New Turkish Family. Koseoglu, Emel; Tepgec, Fatih; YetkIn, Mehmet Fatih; Uyguner, Oya; EkIncI, Ayten; Abdulrezzak, Ummuh Clinical report Mar 1, 2018 2768
De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case. Alhalabi, Nawras; Al-Achkar, Walid; Wafa, Abdulsamad; Kenj, Mazen; Alhalabi, Marwan Clinical report Jan 1, 2018 2817
Patent Omphalomesenteric Duct with Protruding Bowels through a Ruptured Omphalocele. Mammadov, Emil Clinical report Jan 1, 2018 452
A Lucky Accident: Brugada Syndrome Associated with Out-of-Hospital Cardiac Arrest. Lee, Michelle T.; Marah, Naddi Clinical report Jan 1, 2018 1603
Neonatal Stridor in Familial Congenital Laryngeal Paralysis (Plott Syndrome): A Case Study in an Omani Family. Shatla, Emad Sadek; Prashanth, Gowda Parameshwara; Aguiar, Rodney; Shivalingam, Ganji; Haq, Adeel Ah Case study Nov 1, 2017 1849
Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy. Gonc, E. Nazli; Ozon, Alev; Alikasifoglu, Ayfer; Kandemir, Nurgun Case study Sep 1, 2017 3487
Surgical Management of Atresia Ani in Calves. Chethan, G.N.; Maruthi, S.T.; Kumar, M.L. Bharath Clinical report Jul 1, 2017 817
Surgical Management of Atresia Ani in Calves - Comparative Evaluation of Timely and Delayed Presentation Complications. Kumar, P. Ravi; Prasad, V. Devi; Sreenu, M.; Krishna, N.V.V. Hari Clinical report Jul 1, 2017 1921
A Rare Genodermatosis: H Syndrome. Sezer, Ozlem; Ozen, Duriye Sila Karagoz; Demirag, Mehmet Derya; Toto, Ismail; Ozturk, Hacer Pinar; T Case study Jun 1, 2017 375
POU1F1 and PROP1 Gene Mutations in 4 Cases of Combined Pituitary Hormone Deficiency. Akgun, Bilcag; Karademir, Zehra; Isik, Esra; Darcan, Sukran; Aykut, Ayca; Durmaz, Asude; Ozen, Samim Report Jun 1, 2017 344
MEN 2A Family. Pekkolay, Zafer; Soylu, Hikmet; Balsak, Belma Ozlem Tural; Guven, Mehmet; Tuzcu, Alpaslan Kemal Brief article Jun 1, 2017 287
CONRADI-HUNERMANN SYNDROME IN A MALE AND FEMALE CASE WITH TWO NOVEL EBP MUTATIONS. Senturk, LeyliZ; Altunoglu, Umut; Avci, Sahin; Uyguner, Zehra Oya; Karaman, Birsen; Basaran, Seher Report Jun 1, 2017 272
CONGENITAL ANONYCHIA TOTALIS: A RARE OCCURRENCE IN A PAKISTANI FAMILY. Case study Mar 31, 2017 1401
A rare case of lipoid proteinosis. Petkar, Sunil; Galani, Vivek Clinical report Mar 2, 2017 791
Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia. Panzer, Karin; Ekhaguere, Osayame A.; Darbro, Benjamin; Cook, Jennifer; Shchelochkov, Oleg A. Case study Mar 1, 2017 2562
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A). Celmeli, Gamze; Turkkahraman, Doga; Curek, Yusuf; Houghton, Jayne; Akcurin, Sema; Bircan, Iffet Report Mar 1, 2017 3134
HEREDITARY HYPERFERRITINEMIA AND CATARACT SYNDROME: A CASE REPORT. Guler, Ulviye Esra Bayat; Ozcan, Alper; Guler, Yunus; Unal, Ekrem; Per, Huseyin Clinical report Mar 1, 2017 385
CONGENITAL GIANT HEMANGIOMA CASE CAUSING KASABACH MERRITT SYNDROME IN NEONATALS. Ceylan, Mahir; Ozsoy, Nazli Sultan; Ozdemir, Ahmet; Ozcan, Alper; Donmez, Halil; Unal, Ekrem; Gunes, Clinical report Mar 1, 2017 401
Singleton Merten Syndrome: A Rare Cause of Early Onset Aortic Stenosis. Ghadiam, Harshavardhan; Mungee, Sudhir Case study Jan 1, 2017 794
Goldenhar Syndrome with Dextrocardia and Right Pulmonary Hypoplasia: An Unusual Association. Chaudhary, Nagendra; Shrestha, Sandeep; Halwai, Hemant Kumar Clinical report Jan 1, 2017 2089
"Monocept": A Brief Report of Congenital Absence of the Long Head of the Biceps Tendon and Literature Review. Winston, Benjamin A.; Robinson, Katlyn; Crawford, Dennis Clinical report Jan 1, 2017 1208
Scaphoid Fracture in a Patient with a Scaphotrapezial Synostosis: A Case Report and Literature Review. Noureldin, Soliman; Ali, Mohammed; Fallahi, Farshid; Dehler, Thomas Clinical report Jan 1, 2017 1341
Osteopathic Manipulative Treatment Limits Chronic Constipation in a Child with Pitt-Hopkins Syndrome. Aquino, Alessandro; Perini, Mattia; Cosmai, Silvia; Zanon, Silvia; Pisa, Viviana; Castagna, Carmine; Clinical report Jan 1, 2017 3871
Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function. Tsuda, Takeshi; Shillingford, Amanda J.; Vetter, Jane; Kandula, Vinay; Jain, Badal; Temple, Joel Clinical report Jan 1, 2017 2722
Kissing nevus of eyelids - Report of two cases. Report Dec 31, 2016 1191
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family. Dursun, Fatma; Mohamoud, Hussein Sheikh Ali; Karim, Noreen; Naeem, Muhammad; Jelani, Musharraf; Kirm Report Dec 1, 2016 3593
A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report. Prochazkova, Dagmar; Hruba, Zuzana; Konecna, Petra; Skotakova, Jarmila; Fajkusova, Lenka Case study Dec 1, 2016 1076
MIDLINE CLEFT OF LOWER LIP: REVIEW AND CASE REPORTS. Case study Sep 30, 2016 2486
Short Communication - Goldenhar syndrome: a report of rare case with subtle clinical features. Case study Sep 30, 2016 927
Surgical Management of Ocular Dermoid Cyst - A Clinical Study in Eight Calves. Dar, Shahid Hussain; Fazili, Mujeeb Ur Rehman; Dar, Khadim Hussain; Nissar, Shazia; Mir, Abdul Qayoo Clinical report Jul 1, 2016 1360
Surgical Management of Ocular Dermoid and Injury in a Calf. Behera, Sidhartha Sankar; Nayak, Sadananda; Mohanty, Jibanananda Clinical report Jul 1, 2016 1010
Surgical Management of Sclero-Corneal Dermoid in a Dog. Choudhury, M.; Kalita, D. Clinical report Jul 1, 2016 656
Congenital Accessory Tongue and its Surgical Removal in a Calf. Das, Jayakrushna; Pradhan, Snehasis; Sathapathy, Srinivas Clinical report Jul 1, 2016 1019
BILATERAL HYPERMOBILITY OF ULNAR NERVES AT THE ELBOW JOINT WITH UNILATERAL LEFT ULNAR NEUROPATHY IN A COMPUTER USER: A CASE STUDY. Lewanska, Magdalena; Grzegorzewski, Andrzej; Walusiak-Skorupa, Jolanta Case study May 1, 2016 2811
Congenital trypanosomiasis in child born in France to African mother. De Kyvon, Marie-Alix Lestrade-Carluer; Maakaroun-Vermesse, Zoha; Lanotte, Philippe; Priotto, Gerardo Clinical report May 1, 2016 1375
TAR (thrombocytopenia with absent radius) syndrome with congenital acyanotic heart disease: a rare case report. Jagtap, Ashok S.; Gupta, Ankit; Aundhakar, C.D.; Mishra, Lekha; Mahesh, Umardand Clinical report Mar 17, 2016 1015
Unicuspid aortic valve--an uncommon anomaly with a common presentation. Sitwala, Puja; Abusara, Ashraf; Ladia, Vatsal; Panchal, Hemang B.; Raudat, Charles; Paul, Timir K. Clinical report Mar 1, 2016 982
Double-Layered Lateral Meniscus in an 8-Year-Old Child: Report of a Rare Case. Araki, Susumu; Kubo, Mitsuhiko; Kumagai, Kosuke; Imai, Shinji Clinical report Jan 1, 2016 1580
Fatal Meningitis in a 14-Month-Old with Currarino Triad. Qahtani, Hanan Mohammed Al; Aljoqiman, Khalid Suliman; Arabi, Hisham; Shaalan, Hesham Al; Singh, Sum Case study Jan 1, 2016 2644
Hyperemesis gravidarum in undiagnosed Gitelman's syndrome. Acelajado, Maria Czarina; Culpepper, R. Michael; Bolton, Wilburn D., III Case study Jan 1, 2016 2954
Congenital nephrotic syndrome: a diagnostic and management dilemma. Moodley, R.; Naicker, E.; Bhimma, R. Clinical report Nov 1, 2015 2058
Congenital abnormalities of the optic nerve: this first article in a two-part series on optic nerve abnormalities concentrates on congenital conditions with a selection of case studies and short discussion. Lanier, Kate Case study Nov 1, 2015 2860
Bilateral staged total hip replacement and the natural progress of an untreated case of developmental dysplasia (dislocation) of the hip: a clinical case report by the surgeon and the patient. Honarpisheh, Hamid; Ghazavi, Mohammad Taghi Clinical report Jul 1, 2015 2383
Intratympanic membrane congenital cholesteatoma. Sakaida, Hiroshi; Takeuchi, Kazuhiko Case study Jul 1, 2015 476
Klippel-Trenaunay Syndrome accompanied by the findings of scoliosis and spinal nerve root compression due to AVM. Ozkan, Yasemin; Sanal, Bekir Report Jun 1, 2015 2561
Congenital high type anorectal malformation (recto-vaginal fistula) in a 7 months old girl: a case report. Kharnaior, Anderson; Suiyibangbe; Lokendra, K.; Devi, S. Ranita; Moirangthem, G.S. Clinical report Apr 27, 2015 1379
Nerve sparing ventral clitoroplasty: a new treatment for clitoromegaly. Sekhar, Immadi Chandra; Vanaja, G. Apr 2, 2015 1867
Novel mutation in Wolcott-Rallison syndrome with variable expression in two Omani siblings. Sinani, Siham Al-; Yaarubi, Saif Al-; Sharef, S.W.; Murshedi, Fathyia Al-; Maamari, Watfa Al- Clinical report Mar 1, 2015 2251
Retrocaval ureter: a case report. Pankaj, Deepak; Prakash, Sanjay; Singh, Tushar Clinical report Feb 19, 2015 1242
A clinical study on congenital anomalies of breast in Rohilkhand region. Sharan, Jagadamba; Kumar, Kaushal; Raza, Md. Arshad; Srivatsava, Vijai Prakash Clinical report Jan 12, 2015 1424
Rhizomelic Chondrodysplasia punctata: a rare case report. Yashodhara, P.; Elizabeth, B.; Madhavi, N.; Kumar, B. Deeva; Reddy, A. Tirupathi Clinical report Jan 12, 2015 1453
Mounier Kuhn syndrome: a rare cause of bronchiectasis. Khanduri, Sachin; Agrawal, Deepak; Singh, Bhumika; Varshney, Garima; Huda, Fahimul Clinical report Jan 8, 2015 1293
Swallowing evaluation in infants with congenital heart disease and down syndrome: clinical cases study/ Avaliacao da degluticao em lactentes com cardiopatia congenita e sindrome de down: estudo de casos. Fraga, Deborah Fick Bohm; Pereira, Karine da Rosa; Dornelles, Silvia; Olchik, Maira Rosenfeld; Levy, Ensayo Jan 1, 2015 3506
Cherubism. Thompson, Lester D.R. Case study Jan 1, 2015 631
Laparoscopic cholecystectomy in situs inversus with left-sided gall bladder. Neogi, Probal; Singh, Santosh Kumar Clinical report Nov 1, 2014 1231
Fibrodysplasia ossificans progressiva--radiological findings: a case report. Al-Salmi, Ishaq; Raniga, Sameer; Hadidi, Aymen Al- Clinical report Sep 1, 2014 2003
Multiple congenital malformations of female internal genitalia: its surgical correction. Mishra, Ritu; Misra, Aditya Prakash Clinical report Aug 11, 2014 1345
Dandy-walker malformation: A rare congenital anomaly. Fatima, Uroos; Arakeri, Satish; R., Ram Kumar K.; K., Roopa Clinical report Aug 4, 2014 1599
Bland-White-Garland syndrome: value of computed tomographic angiography. Ziadi, Marla C.; Diodato, Luis; Ameriso, Jose L.; Villavicencio, Roberto L. Clinical report Aug 1, 2014 588
Reinnervation of facial muscles with only a cross-facial nerve graft in a 25-year-old patient with congenital facial palsy. Seyed-Forootan, Kamal; Karimi, Hamid; Hasani, Esmaiil Case study Jul 1, 2014 110
Heterotaxy syndrome with polysplenia. Winter, Bart J.; Reidman, Daniel A.; Statler, John Clinical report Jul 1, 2014 1164
Bilateral Tessier cleft 3: a case report. Bordoloi, Utpal Clinical report Jun 23, 2014 1243
Late presentation of congenital diaphragmatic hernia: a case report. Al Ghafri, Mohammed; Al Sidairi, Ibtisam; Nayar, Madhavan Case study May 1, 2014 1265
Cystic hygroma in adults-a rare case report. Mallick, Krushna Chandra; Khatua, Rabindra Kumar; Routray, Subhalaxmi; Lenka, Anasuya Case study Mar 10, 2014 1241
Prenatal diagnosis of granular cell tumor. Kadivar, Maliheh; Sangsari, Razieh; Alavi, Azin Case study Mar 1, 2014 1843
Pulmonary aplasia with unusual associations in a woman. Bachh, Arshad Altaf; Pulluri, Sridhar; Beigh, Aadil; Raju, Chippa; Deshpande, Ranganath Case study Mar 1, 2014 1439
Accessory spleen--a case report with a brief review. Devi, Keisam Anupama; Chinglensana, Laitonjam Feb 24, 2014 1723
Uncommon cause of paradoxical embolism in a case of scimitar syndrome. Alabi, Fortune O.; Umeh, Fred; Lama, Maximo; Christian, Francis G. Case study Jan 1, 2014 1412
Clinical approach to a suspected case of first branchial arch syndrome. Yamaguchi, Noboru; Nakamura, Shiho; Yamaza, Haruyoshi; Nishigaki, Soichiro; Masuda, Keiji; Yanagita, Case study Jan 1, 2014 2164
Scalp-ear-nipple syndrome: a case report. Morales-Peralta, Estela; Andres, Vivian; Betancourt, Daine Campillo Case study Jan 1, 2014 1036
MEN1 syndrome and hibernoma: an uncommonly recognised association? Hedayati, Venus; Thway, Khin; Thomas, J. Meirion; Moskovic, Eleanor Case study Jan 1, 2014 1841
M to T rearrangement: an approach to correct webbed neck deformity. Murthy, Ananth S.; McGraw, Margeaux Case study Jan 1, 2014 1586
Mother-to-child transmission of congenital Chagas disease, Japan. Imai, Kazuo; Maeda, Takuya; Sayama, Yusuke; Mikita, Kei; Fujikura, Yuji; Misawa, Kazuhisa; Nagumo, M Clinical report Jan 1, 2014 1952
Acrokeratoses verruciformis of HOPF: an association with polymorphic light eruption. Ramesh, M.; Ramya, N.; Gopal, M.G.; Kumar B.C., Sharath; Nandini, A.S. Clinical report Dec 2, 2013 1380
An interesting rare case of benign congenital oesophago-bronchial fistula presenting in adulthood--a case report. M., Narayan; Dilip, Devershi Ajay; Ravindra, Chandankhede Abhijit Clinical report Oct 21, 2013 1574
A case report on septate uterus. Vasudha; Anitha; Syamala; Usharani Clinical report Sep 16, 2013 1063
A child with progressive enlargement of the left foot. Gilbert, Patrick; Serou, Michael; Neitzschman, Harold R. Report Jul 1, 2013 728
Congenital absence of inferior vena cava with idiopathic deep vein thrombosis in an adult. Hooda, Deepak; Penumetsa, Karthik; Jackson, Timothy; Gharib, Wissam; Beto, Robert J.; Warden, Bradfo Case study Mar 1, 2013 1035
The difficulties in teaching an adult with congenital blindness to draw cubes: a case study. Chang, Wan-Chi; Bin, I. Report Mar 1, 2013 2583
Mermaid baby with multiple congenital anomalies in monochorionic twin gestation in diabetic mother. C., Meenal.; B., Hiremath P.; Bansal, Nidhi; Subhasini; Premaleela; Rajesh; Ravikannan Clinical report Jan 7, 2013 942
Congenital sialoblastoma of the accessory parotid gland. Parag, P. Clinical report Dec 1, 2012 737
Ocular problems in triple-A syndrome and their management/Triple A sendromlu bir olgudaki goz problemleri ve tedavi yaklasimi. Okumus, Seydi; Coskun, Erol; Erbagci, Ibrahim; Erbagci, Zulal; Gulsen, Murat Taner; Akarsu, Ersin; B Case study Nov 1, 2012 1796
Diagnosis of microvillous inclusion disease: a case report and literature review with significance for Oman. Al-Sinani, Siham; Sharef, Sharef Waadallah; Lakhtakia, Ritu; Abdellatif, Mohamed Case study Nov 1, 2012 2528
REPAIR OF BILATERAL CONGENITAL UPPER EYELID COLOBOMA- A CASE REPORT. Sheikh, Muhammad Muneeb Clinical report Mar 31, 2012 1386
Inner ear malformations in siblings presenting with vestibular symptoms in early childhood. Butler, I.R.T.; Seedat, R.Y. Case study Sep 1, 2011 2067
Case report: infantile systemic hyalinosis: a dental perspective. Olczak-Kowalczyk, D.; Krasuska-Stawinska, E.; Rokicki, D.; Pronicki, M. Report Aug 1, 2011 2004
Beware the bifid rib! Scheepers, Shaun; Andronikou, Savvas Clinical report Dec 1, 2010 531
Case report: rehabilitation of a child with dentinogenesis imperfecta and congenitally missing lateral incisors. Millet, C.; Viennot, S.; Duprez, J.P. Case study Oct 1, 2010 3005
A rare congenital midline cervical cleft. Warden, C.; Millar, A.J.W. Case study Aug 1, 2010 852
Inverted liver with suprahepatic, anteriorly displaced gallbladder. Hibbs, Harold; Ahmad, Usman Case study May 1, 2010 807
Interaction coaching with mothers of children with congenital deaf-blindness at home: applying the diagnostic intervention model. Janssen, Marleen J.; Riksen-Walraven, J. Marianne; van Dijk, Jan P.M.; Ruijssenaars, Wied A.J.J.M. Report Jan 1, 2010 5984
Bilateral congenital trigger thumb: a case report and discussion of management. Schessler, Matthew J.; McClellan, W. Thomas Case study Nov 1, 2009 1225
Diastematomyelia--a case report/ Diastematomyeli: bir olgu sunumu. Turcan, Ayten; Umut, Saadet Yazgan; Sariyildiz, Mustafa Akif Case study Jun 1, 2009 1085
Laryngeal saccular cyst in an infant. Pereira, Kevin D. Case study Jan 1, 2009 770
An unusual Brugada syndrome case/nadir gorulen bir Brugada sendromu vakasi. Orem, Cihan; Kiris, Gulhanim; Durmus, Ismet; Kaplan, Sahin; Gedikli, Omer; Baykan, Merih; Gokce, Mus Case study Oct 1, 2008 1269
A rare cause of dilated cardiomyopathy; Alstrom syndrome/Dilate kardiyomiyopatinin nadir bir nedeni; Alstrom sendromu. Unlu, Cihan; Ustun, Ihsan; Akay, Fahrettin; Dogan, Umuttan Letter to the editor Aug 1, 2008 805
Sindrome de Berardinelli. reporte de un caso con evolucion fatal. Daher, Elizabeth; Silva, Geraldo, Jr.; Benevides, Veronica; Mendonca, Patricia; Bezerra, Helder; Sil Jun 1, 2008 2068
Seventh cervical rib associated with subclavian artery occlusion and multiple infarcts: case report. Wise, Roxanne Case study Jun 1, 2008 2279
Congenital midline cervical cleft: a report of two cases. Franzese, Christine; Hayes, James D.; Nichols, Kristie Report Mar 1, 2008 2064
Anaesthesia and Alstrom's syndrome. Lynch, G.; Clinton, S.; Siotia, A. Clinical report Apr 1, 2007 678
Congenital midline cervical cleft: a report of 3 cases. Wood, W. Edward Feb 1, 2006 1698
Diagnostic dilemma. Oct 1, 2004 609

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