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Problemy Tuberkuleza I Boleznei Legkikh
|
December 10, 2008
[Use of an endobronchial valve in complex treatment of patients with infiltrative pulmonary tuberculosis]
A V Levin, E A Tseĭmakh, P E Zimonin, et al.
American Journal of Medical Genetics. Part A
|
February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation
C P Barnett, R Mendoza-Londono, S Blaser, et al.
AJNR. American Journal of Neuroradiology
|
April 1, 1996
Abnormal ocular enhancement in Sturge-Weber syndrome: correlation of ocular MR and CT findings with clinical and intracranial imaging findings
P D Griffiths, M B Boodram, S Blaser, et al.
Ophthalmology
|
November 1, 1992
Retinal findings after head trauma in infants and young children
Y M Buys, A V Levin, R W Enzenauer, et al.
Angiologiia I Sosudistaia Khirurgiia = Angiology and Vascular Surgery
|
March 4, 2026
[Successful treatment of a patient with ruptured abdominal aortic aneurysm, COVID-19, and prosthesis infection (case report)]
A S Igoshin, Yu V Karabach, A Yu Volkov, et al.
Human Genetics
|
December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13
G B Collin, J D Marshall, C F Boerkoel, et al.
Rheumatology (Oxford, England)
|
February 8, 2006
Tumour necrosis factor alpha inhibitors in the treatment of childhood uveitis
R K Saurenmann, A V Levin, J B Rose, et al.
The Journal of Pediatrics
|
February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy
J L Michaud, E Héon, F Guilbert, et al.
American Journal of Medical Genetics
|
June 22, 1999
Early-infantile galactosialidosis: prenatal presentation and postnatal follow-up
M S Patel, J W Callahan, S Zhang, et al.
Human Mutation
|
January 1, 1997
Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1)
R A Spritz, J Oh, K Fukai, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 83) with videos related to
Sort By:
Page
of 9
Problemy Tuberkuleza I Boleznei Legkikh
|
December 10, 2008
[Use of an endobronchial valve in complex treatment of patients with infiltrative pulmonary tuberculosis]
A V Levin, E A Tseĭmakh, P E Zimonin, et al.
American Journal of Medical Genetics. Part A
|
February 12, 2009
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation
C P Barnett, R Mendoza-Londono, S Blaser, et al.
AJNR. American Journal of Neuroradiology
|
April 1, 1996
Abnormal ocular enhancement in Sturge-Weber syndrome: correlation of ocular MR and CT findings with clinical and intracranial imaging findings
P D Griffiths, M B Boodram, S Blaser, et al.
Ophthalmology
|
November 1, 1992
Retinal findings after head trauma in infants and young children
Y M Buys, A V Levin, R W Enzenauer, et al.
Angiologiia I Sosudistaia Khirurgiia = Angiology and Vascular Surgery
|
March 4, 2026
[Successful treatment of a patient with ruptured abdominal aortic aneurysm, COVID-19, and prosthesis infection (case report)]
A S Igoshin, Yu V Karabach, A Yu Volkov, et al.
Human Genetics
|
December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13
G B Collin, J D Marshall, C F Boerkoel, et al.
Rheumatology (Oxford, England)
|
February 8, 2006
Tumour necrosis factor alpha inhibitors in the treatment of childhood uveitis
R K Saurenmann, A V Levin, J B Rose, et al.
The Journal of Pediatrics
|
February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy
J L Michaud, E Héon, F Guilbert, et al.
American Journal of Medical Genetics
|
June 22, 1999
Early-infantile galactosialidosis: prenatal presentation and postnatal follow-up
M S Patel, J W Callahan, S Zhang, et al.
Human Mutation
|
January 1, 1997
Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1)
R A Spritz, J Oh, K Fukai, et al.
Page
of 9