scholarly journals Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: Case report

2011 ◽  
Vol 12 (1) ◽  
Author(s):  
Giovana T Torrezan ◽  
Felipe CC da Silva ◽  
Ana CV Krepischi ◽  
Érika MM Santos ◽  
Fábio de O Ferreira ◽  
...  
Keyword(s):  
Case Report ◽  
Patient Case ◽  
Intragenic Deletion

Multiple Skull Base Meningiomata in a Transgender Patient: Case Report and Literature Review

2019 ◽  
Author(s):  
Andrew Alalade ◽  
Christopher Millward ◽  
Piyali Pal ◽  
Catherine Gilkes
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Skull Base ◽  
Patient Case ◽  
Transgender Patient

Auto immune hypoglycemia in individuals with type 1 diabetes, from a patient case report

2019 ◽  
Author(s):  
Rolly Junior Louzolo-Kimbembe ◽  
Ghizlane El Mghari ◽  
Nawal El Ansari
Keyword(s):  
Type 1 Diabetes ◽  
Case Report ◽  
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Rare NRAS mutation causing Noonan syndrome type 6 in a Saudi patient: case report

2021 ◽  
pp. 413-415
Author(s):  
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Anfal Alsultan ◽  
Halah AlMuhaidib ◽  
Sarah Aldhahri ◽  
Dalal Bubshait
Keyword(s):  
Case Report ◽  
Noonan Syndrome ◽  
Syndrome Type ◽  
Patient Case ◽  
Nras Mutation

DOENÇA ARTERIAL OBSTRUTIVA PERIFÉRICA E NEUROPATIA EM PACIENTE DIABÉTICO TIPO II: RELATO DE CASO / PERIPHERAL OBSTRUCTIVE ARTERIAL DISEASE AND NEUROPATHY IN TYPE II DIABETIC PATIENT: CASE REPORT

2020 ◽  
Vol 6 (9) ◽  
pp. 71910-71917
Author(s):  
Renata Cristina Taveira Azevedo ◽  
Carolina Mendes Ferreira ◽  
André Almeida Brito ◽  
Isabella Viana Araujo ◽  
Paula Chaves Barbosa ◽  
...  
Keyword(s):  
Case Report ◽  
Diabetic Patient ◽  
Arterial Disease ◽  
Type Ii ◽  
Patient Case

scholarly journals Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
Vincenzo Altieri ◽  
Oronzo Capozzi ◽  
Maria Cristina Marzano ◽  
Oriana Catapano ◽  
Immacolata Di Biase ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Molecular Characterization ◽  
Marker Chromosome
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