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M Brandis

Showing results (141-150 of 158) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1996
Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13F Hildebrandt, M Cybulla, B Strahm, et al.
Medical and Pediatric Oncology|April 1, 1997
Renal function after conditioning therapy for bone marrow transplantation in childhoodL Patzer, L Hempel, F Ringelmann, et al.
Klinische Wochenschrift|November 15, 1988
Cyclosporin A treatment in children with minimal change nephrotic syndrome and focal segmental glomerulosclerosisJ Brodehl, M Brandis, U Helmchen, et al.
Immunodeficiency|January 1, 1993
Primary severe immunodeficiency due to impaired signal transduction in T cellsM Schlesier, C Niemeyer, U Duffner, et al.
European Journal of Pediatrics|March 21, 1998
Acute bilateral renal vein thrombosis complicating Netherton syndromeM Pohl, L B Zimmerhackl, I Hausser, et al.
American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneH Omran, K Häffner, A Völkel, et al.
Pediatric Research|October 17, 1998
Plasma levels and gene expression of granulocyte colony-stimulating factor, tumor necrosis factor-alpha, interleukin (IL)-1beta, IL-6, IL-8, and soluble intercellular adhesion molecule-1 in neonatal early onset sepsisR Berner, C M Niemeyer, J U Leititis, et al.
American Journal of Human Genetics|January 13, 2000
Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigreeH Omran, C Fernandez, M Jung, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische NephrologieF Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunctionH Mitsumoto, M Davidson, D Moore, et al.
Pageof 16

Showing results (141-150 of 158) with videos related to

Sort By:
Pageof 16
Cytogenetics and Cell Genetics|January 1, 1996
Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13F Hildebrandt, M Cybulla, B Strahm, et al.
Medical and Pediatric Oncology|April 1, 1997
Renal function after conditioning therapy for bone marrow transplantation in childhoodL Patzer, L Hempel, F Ringelmann, et al.
Klinische Wochenschrift|November 15, 1988
Cyclosporin A treatment in children with minimal change nephrotic syndrome and focal segmental glomerulosclerosisJ Brodehl, M Brandis, U Helmchen, et al.
Immunodeficiency|January 1, 1993
Primary severe immunodeficiency due to impaired signal transduction in T cellsM Schlesier, C Niemeyer, U Duffner, et al.
European Journal of Pediatrics|March 21, 1998
Acute bilateral renal vein thrombosis complicating Netherton syndromeM Pohl, L B Zimmerhackl, I Hausser, et al.
American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate geneH Omran, K Häffner, A Völkel, et al.
Pediatric Research|October 17, 1998
Plasma levels and gene expression of granulocyte colony-stimulating factor, tumor necrosis factor-alpha, interleukin (IL)-1beta, IL-6, IL-8, and soluble intercellular adhesion molecule-1 in neonatal early onset sepsisR Berner, C M Niemeyer, J U Leititis, et al.
American Journal of Human Genetics|January 13, 2000
Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigreeH Omran, C Fernandez, M Jung, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische NephrologieF Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunctionH Mitsumoto, M Davidson, D Moore, et al.
Pageof 16