Ahmed Abdalazim Dafallah Albashir

ORCID: 0000-0001-9321-489X
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About
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Research Areas
  • COVID-19 Clinical Research Studies
  • Malaria Research and Control
  • Genetic Syndromes and Imprinting
  • Genetic and Kidney Cyst Diseases
  • Erythropoietin and Anemia Treatment
  • Dialysis and Renal Disease Management
  • Mosquito-borne diseases and control
  • Fetal and Pediatric Neurological Disorders
  • Long-Term Effects of COVID-19
  • Infant Health and Development
  • Respiratory Support and Mechanisms
  • Tracheal and airway disorders
  • Hemoglobinopathies and Related Disorders
  • Genetic factors in colorectal cancer
  • Pericarditis and Cardiac Tamponade
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Pulmonary Hypertension Research and Treatments
  • Ear and Head Tumors
  • Acute Kidney Injury Research
  • Neonatal Health and Biochemistry
  • Renal and related cancers
  • Pediatric health and respiratory diseases
  • Vascular Anomalies and Treatments
  • Acute Myocardial Infarction Research
  • Cardiovascular Health and Risk Factors

University of Gezira
2019-2022

Wad Medani Ahlia University
2020-2021

Ministry of Health
1997

Médecins Sans Frontières
1995

Asymptomatic oral candidal carriage has been extensively studied in adults, but only rarely infants. The present investigation aimed to determine the asymptomatic of species healthy infants and its relationship age, sex, feeding pattern use a pacifier. swab technique was used for isolation. Candidal were isolated from 48% without significant gender or between breast-fed bottle-fed Similarly, history maternal vaginal candidosis, presence nappy rash, had no carriage. Infants who routinely...

10.1111/j.1600-0714.1995.tb01200.x article EN Journal of Oral Pathology and Medicine 1995-09-01

Bardet-Biedl syndrome is a rare multisystem autosomal recessive disorder that falls under the spectrum of ciliopathy disorders. It characterized by rod-cone dystrophy, renal malformations, polydactyly, learning difficulties, central obesity, and hypogonadism. Many minor features are related with might aid in diagnosis crucial clinical management. diagnosed on basis signs symptoms, which can be confirmed genetic testing. Here we present four cases syndrome. To our knowledge, these first...

10.1186/s13256-022-03396-6 article EN cc-by Journal of Medical Case Reports 2022-04-28

Kuwait is a desert country where the prevailing high temperatures, low humidity, and scant vegetation suggest prevalence of allergy. We evaluated atopic sensitization (presence allergen‐specific IgE) among young adult blood donors by screening total 505 subjects (male : female ratio 1.6) with mean age 28.4 years (range 18–50 years). The Pharmacia CAP‐Phadiatop® test, which detects serum IgE specific to most common airborne allergens, was used. Some sensitizing allergens were also identified...

10.1111/j.1398-9995.1997.tb02523.x article EN Allergy 1997-12-01

Colorectal cancer is a common type of worldwide, including in Sudan. However, few studies have assessed its demographic, clinical and pathological patterns the Sudanese population.To assess patients with colorectal at National Cancer Institute, University Gezira, Sudan.This retrospective, cross-sectional study analyzed data all who presented to between January 2016 December 2017. one two Institutes Sudan receives from across The information were extracted patients' files.A total 163...

10.4103/sjmms.sjmms_138_18 article EN cc-by-nc-sa Saudi Journal of Medicine and Medical Sciences 2019-01-01

Beta-2-microglobulin (beta2-m) has been proposed as a marker of middle molecules to assess one aspect the efficacy dialysis. Until now, few data have published about extra renal (metabolic) clearance and generation rates beta2-microglobulin, which are necessary for calculation total mass removal beta2-m in hemodialysis patients. We developed simple method derive by measuring pre post dialysis blood concentrations using kinetic modeling. Ten stable patients were included this study. Pre...

10.1097/00002480-200111000-00011 article EN ASAIO Journal 2001-11-01

ABSTRACT Frank’ sign or diagonal earlobe crease (DELC) is a that extends backwards from the tragus at an angle of 45 degree across lobule to ear edge auricle. It has been described as dermatological marker for coronary artery disease. Frank’s useful clinical Inspection earlobes should be considered integral part physical examination in practice patients with suspected

10.1093/omcr/omab089 article EN cc-by-nc Oxford Medical Case Reports 2021-09-01

Acute pericarditis and pericardial effusion are rare extrapulmonary presentations of COVID-19. They can occur without concomitant pulmonary disease or myocardial injury. A high index suspicion is necessary to assure early diagnosis treatment.

10.22541/au.159969834.49964606 preprint EN Authorea (Authorea) 2020-09-10

Coronary interventions in patients of achondroplasia have been reported rarely the medical literature. Due to short stature and kyphoscoliosis, endovascular access (Cannulation) coronary arteries is usually extremely difficult such patients.A 33 years old patient, a known case achondroplasia, presented with epigastric pain for 3 h duration university hospital, Sudan. Her height was 95 cm her weight 38 Kg. A trans-femoral approach angioplasty preferred. After it has cannulate left system at...

10.1186/s12872-020-01612-z article EN cc-by BMC Cardiovascular Disorders 2020-07-10

Abstract Malaria is the most common tropical disease in Sudan, which caused by an infection with Plasmodium protozoa transmitted infective female Anopheles mosquito. Headache, fever, cough, fatigue, malaise, shaking chills, arthralgia and myalgia are cardinal features of malaria, but occasionally, it has atypical presentation. Intestinal obstruction as a complication extremely rare Here within, we describe 28-year-old Sudanese man who presented colicky abdominal pain, absolute constipation...

10.1093/omcr/omaa098 article EN cc-by-nc Oxford Medical Case Reports 2020-10-01

Hereditary hemorrhagic telangiectasia (HHT) also known as Osler-Weber-Rendu syndrome is a rare autosomal dominant disorder, which results in vascular dysplasia affecting mainly visceral and mucocutaneous organs. Case Presentation. A 65-year-old woman with 12-year history of recurrent spontaneous epistaxis presented shortness breath, easy fatigability, bilateral lower limb edema. Her family was significant for definite hereditary first-degree relatives. During the previous 15 days, she has...

10.1155/2020/6395629 article EN cc-by Case Reports in Medicine 2020-12-14

Abstract: Bardet–Biedl syndrome is a rare autosomal recessive disorder falls under the spectrum of ciliopathy disorders. Its characterized by rod-cone dystrophy, renal malformations, postaxial polydactyly, learning difficulties, central obesity and hypogonadism. Hyponatremia, hepatic haemangioma, gall bladder stones subclinical hypothyroidism rarely described in literature as clinical presentations BBS.

10.22541/au.160654867.72853157/v1 preprint EN Authorea (Authorea) 2020-11-28

Introduction: Beta-2-microglobulin (β2-M) has been proposed as a marker of middle molecules to assess the efficacy dialysis. Only few data have published about extra renal clearance and generation rate β2-microglobulin which are necessary for calculation total mass removal β2-M in hemodialysis patients. Here we developed simple method derive from measuring pre-and post-dialysis blood concentrations using kinetic modelling. Methods: Ten stable patients included this study. Pre- were measured...

10.1097/00002480-200003000-00264 article EN ASAIO Journal 2000-03-01
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