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Gut
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February 14, 2006
Chewing is an important first step in digestion. Diagnosis: piece of glass in stomach
R Slim, K Honein, C Yaghi, et al.
Le Journal Medical Libanais. the Lebanese Medical Journal
|
October 12, 2000
[Hemostatic embolization of hepatocellular carcinoma complicated by hemoperitoneum. Apropos of 2 cases and review of the literature]
J Boujaoude, B Abboud, S Slaba, et al.
Clinical Genetics
|
October 7, 1998
Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers
Y B Mouglabey, S Nimri, F Sayegh, et al.
Acta Radiologica (Stockholm, Sweden : 1987)
|
April 16, 2003
Adrenal adenoma in a patient with Gardner's syndrome. A case report
K Chelaïfa, K Bouzaïdi, S Chouaïb, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1992
The neurofibromatosis 1 gene transcripts expressed in peripheral nerve and neurofibromas bear the additional exon located in the GAP domain
C Teinturier, G Danglot, R Slim, et al.
Human Genetics
|
September 10, 1999
A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution
M N Helwani, M Seoud, L Zahed, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
July 5, 2003
[Tuberculous meningitis with pituitary abscess]
K Chelaïfa, K Bouzaïdi, O Azaïz, et al.
Journal De Radiologie
|
April 1, 1979
[Radiographic appearances of a renin secreting renal tumor. A rare cause of hypertension (author's transl)]
R Slim, A El Materi, H Ben Maiz, et al.
Journal of the Society for Gynecologic Investigation
|
October 26, 2001
The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies
I B Van den Veyver, B Norman, C Q Tran, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
June 25, 2005
[Lipoma of the skull base. A case report]
K Nouira, H Hila, A Mekni, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 80) with videos related to
Sort By:
Page
of 8
Gut
|
February 14, 2006
Chewing is an important first step in digestion. Diagnosis: piece of glass in stomach
R Slim, K Honein, C Yaghi, et al.
Le Journal Medical Libanais. the Lebanese Medical Journal
|
October 12, 2000
[Hemostatic embolization of hepatocellular carcinoma complicated by hemoperitoneum. Apropos of 2 cases and review of the literature]
J Boujaoude, B Abboud, S Slaba, et al.
Clinical Genetics
|
October 7, 1998
Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers
Y B Mouglabey, S Nimri, F Sayegh, et al.
Acta Radiologica (Stockholm, Sweden : 1987)
|
April 16, 2003
Adrenal adenoma in a patient with Gardner's syndrome. A case report
K Chelaïfa, K Bouzaïdi, S Chouaïb, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1992
The neurofibromatosis 1 gene transcripts expressed in peripheral nerve and neurofibromas bear the additional exon located in the GAP domain
C Teinturier, G Danglot, R Slim, et al.
Human Genetics
|
September 10, 1999
A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution
M N Helwani, M Seoud, L Zahed, et al.
Journal of Neuroradiology = Journal De Neuroradiologie
|
July 5, 2003
[Tuberculous meningitis with pituitary abscess]
K Chelaïfa, K Bouzaïdi, O Azaïz, et al.
Journal De Radiologie
|
April 1, 1979
[Radiographic appearances of a renin secreting renal tumor. A rare cause of hypertension (author's transl)]
R Slim, A El Materi, H Ben Maiz, et al.
Journal of the Society for Gynecologic Investigation
|
October 26, 2001
The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies
I B Van den Veyver, B Norman, C Q Tran, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
June 25, 2005
[Lipoma of the skull base. A case report]
K Nouira, H Hila, A Mekni, et al.
Page
of 8