J Bircher|J P Colombo - JoVE Visualize

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Journal of Hepatology|January 1, 1992

Higher levels of serum aminoterminal type III procollagen peptide, and laminin in alcoholic than in nonalcoholic cirrhosis of equal severityE Lotterer, A M Gressner, J Kropf, et al.

Neurochemical Research|October 1, 1990

Brain development: 1H magnetic resonance spectroscopy of rat brain extracts compared with chromatographic methodsR Burri, P Bigler, P Straehl, et al.

European Journal of Pediatrics|March 1, 1991

N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxicationG Schubiger, C Bachmann, P Barben, et al.

Padiatrie Und Padologie|January 1, 1982

[Lethal neonatal deficiency of carbamyl phosphate synthetase (author's transl)]E Plöchl, C Bachmann, O Stöllinger, et al.

Human Mutation|August 26, 1998

Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1U Finckh, A Kohlschütter, H Schäfer, et al.

Contact Dermatitis|March 27, 2018

Delayed-type allergy to cobalt-comparison of a flow cytometric lymphocyte proliferation test with patch testingIris Spoerri, Andreas J Bircher, Susanne Link, et al.

Molecular and Chemical Neuropathology|August 1, 1990

Reduced myelinogenesis and recovery in hyperphenylalaninemic rats. Correlation between brain phenylalanine levels, characteristic brain enzymes for myelination, and brain developmentR Burri, C Steffen, S Stieger, et al.

Allergy|April 1, 1997

Angiotensin-converting enzyme inhibitor-induced angioedema: late onset, irregular course, and potential role of triggersP I Schiller, S L Messmer, W E Haefeli, et al.

A & a Case Reports|January 23, 2015

Severe anaphylactic shock due to ethylene oxide in a patient with myelomeningocele: successful exposure prevention and pretreatment with omalizumabAdrian Listyo, Kathrin Scherer Hofmeier, Oliver Bandschapp, et al.

Human Genetics|August 1, 1992

Ornithine transcarbamylase (OTC) deficiency in a female patient with a de nova deletion of the paternal X chromosomeR Slomski, I Braulke, C Behrend, et al.

Pageof 32

Showing results (241-250 of 316) with videos related to

Sort By:

Pageof 32

Journal of Hepatology|January 1, 1992

Higher levels of serum aminoterminal type III procollagen peptide, and laminin in alcoholic than in nonalcoholic cirrhosis of equal severityE Lotterer, A M Gressner, J Kropf, et al.

Neurochemical Research|October 1, 1990

Brain development: 1H magnetic resonance spectroscopy of rat brain extracts compared with chromatographic methodsR Burri, P Bigler, P Straehl, et al.

European Journal of Pediatrics|March 1, 1991

N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxicationG Schubiger, C Bachmann, P Barben, et al.

Padiatrie Und Padologie|January 1, 1982

[Lethal neonatal deficiency of carbamyl phosphate synthetase (author's transl)]E Plöchl, C Bachmann, O Stöllinger, et al.

Human Mutation|August 26, 1998

Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1U Finckh, A Kohlschütter, H Schäfer, et al.

Contact Dermatitis|March 27, 2018

Delayed-type allergy to cobalt-comparison of a flow cytometric lymphocyte proliferation test with patch testingIris Spoerri, Andreas J Bircher, Susanne Link, et al.

Molecular and Chemical Neuropathology|August 1, 1990

Reduced myelinogenesis and recovery in hyperphenylalaninemic rats. Correlation between brain phenylalanine levels, characteristic brain enzymes for myelination, and brain developmentR Burri, C Steffen, S Stieger, et al.

Allergy|April 1, 1997

Angiotensin-converting enzyme inhibitor-induced angioedema: late onset, irregular course, and potential role of triggersP I Schiller, S L Messmer, W E Haefeli, et al.

A & a Case Reports|January 23, 2015

Severe anaphylactic shock due to ethylene oxide in a patient with myelomeningocele: successful exposure prevention and pretreatment with omalizumabAdrian Listyo, Kathrin Scherer Hofmeier, Oliver Bandschapp, et al.

Human Genetics|August 1, 1992

Ornithine transcarbamylase (OTC) deficiency in a female patient with a de nova deletion of the paternal X chromosomeR Slomski, I Braulke, C Behrend, et al.

Pageof 32