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Journal of the Royal Society of Health
|
August 1, 1992
Cerebral neurocysticercosis--case report and review
R K Pejaver
Indian Journal of Pediatrics
|
March 27, 2001
An audit of phototherapy units
R K Pejaver, J Vishwanath
The British Journal of Clinical Practice
|
July 1, 1995
Pituitary microadenoma in Turner's syndrome
R K Pejaver, A H Watson
Indian Pediatrics
|
June 1, 1997
Osteopenia of prematurity
R K Pejaver, I al Hifzi
Respiratory Medicine
|
April 1, 1994
Castleman's disease
R K Pejaver, A H Watson
Journal of Inherited Metabolic Disease
|
January 1, 1992
5-Oxoprolinuria due to glutathione synthetase deficiency
R K Pejaver, A H Watson
Journal of the Royal Society of Medicine
|
March 1, 1994
Glutathione synthetase deficiency: a family report
R K Pejaver, A H Watson
Journal of the Royal Society of Medicine
|
September 1, 1995
Parental presence during procedures: a survey of attitudes amongst paediatricians
R K Pejaver, H J Russell
Journal of Inherited Metabolic Disease
|
January 1, 1994
High-dose vitamin E therapy in glutathione synthetase deficiency
R K Pejaver, A H Watson
Journal of the Royal Society of Health
|
June 1, 1995
Sickle cell anaemia in Saudi-Arabian children
R K Pejaver, F Ahmad, H Bedawi
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Journal of the Royal Society of Health
|
August 1, 1992
Cerebral neurocysticercosis--case report and review
R K Pejaver
Indian Journal of Pediatrics
|
March 27, 2001
An audit of phototherapy units
R K Pejaver, J Vishwanath
The British Journal of Clinical Practice
|
July 1, 1995
Pituitary microadenoma in Turner's syndrome
R K Pejaver, A H Watson
Indian Pediatrics
|
June 1, 1997
Osteopenia of prematurity
R K Pejaver, I al Hifzi
Respiratory Medicine
|
April 1, 1994
Castleman's disease
R K Pejaver, A H Watson
Journal of Inherited Metabolic Disease
|
January 1, 1992
5-Oxoprolinuria due to glutathione synthetase deficiency
R K Pejaver, A H Watson
Journal of the Royal Society of Medicine
|
March 1, 1994
Glutathione synthetase deficiency: a family report
R K Pejaver, A H Watson
Journal of the Royal Society of Medicine
|
September 1, 1995
Parental presence during procedures: a survey of attitudes amongst paediatricians
R K Pejaver, H J Russell
Journal of Inherited Metabolic Disease
|
January 1, 1994
High-dose vitamin E therapy in glutathione synthetase deficiency
R K Pejaver, A H Watson
Journal of the Royal Society of Health
|
June 1, 1995
Sickle cell anaemia in Saudi-Arabian children
R K Pejaver, F Ahmad, H Bedawi
Page
of 2