M Haltia|H Kalimo - JoVE Visualize

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Annals of Neurology|April 1, 1984

Neuronal intranuclear inclusion disease in identical twinsM Haltia, H Somer, J Palo, et al.

FEBS Letters|September 6, 1993

Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosisJ Tyynelä, D N Palmer, M Baumann, et al.

Brain Pathology (Zurich, Switzerland)|July 1, 1996

Neuronal ceroid-lipofuscinosis--late-infantile or Jansky-Bielschowsky type--revisitedH H Goebel, L Gerhard, E Kominami, et al.

Acta Neurochirurgica|January 1, 1986

Hormone treatment of meningiomas: lack of response to medroxyprogesterone acetate (MPA). A pilot study of five casesJ Jääskeläinen, E Laasonen, J Kärkkäinen, et al.

American Journal of Medical Genetics|February 15, 1992

Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1pI Järvelä, P Santavuori, L Puhakka, et al.

Investigative Ophthalmology & Visual Science|September 1, 1994

Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndromeT Kivelä, A Tarkkanen, B Frangione, et al.

Surgical Neurology|March 1, 1985

Intracranial hemangiopericytoma: radiology, surgery, radiotherapy, and outcome in 21 patientsJ Jääskeläinen, A Servo, M Haltia, et al.

Acta Neuropathologica|January 1, 1988

A transient hypertensive opening of the blood-brain barrier can lead to brain damage. Extravasation of serum proteins and cellular changes in rats subjected to aortic compressionT E Sokrab, B B Johansson, H Kalimo, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|December 18, 2003

Mast cells and IgE-containing cells in gastric mucosa of Helicobacter pylori infected and non-infected patients with chronic urticariaM Liutu, K Kalimo, H Kalimo, et al.

Neuromuscular Disorders : NMD|October 1, 1996

Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutationT Tyni, A Majander, H Kalimo, et al.

Pageof 34

Showing results (121-130 of 334) with videos related to

Sort By:

Pageof 34

Annals of Neurology|April 1, 1984

Neuronal intranuclear inclusion disease in identical twinsM Haltia, H Somer, J Palo, et al.

FEBS Letters|September 6, 1993

Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosisJ Tyynelä, D N Palmer, M Baumann, et al.

Brain Pathology (Zurich, Switzerland)|July 1, 1996

Neuronal ceroid-lipofuscinosis--late-infantile or Jansky-Bielschowsky type--revisitedH H Goebel, L Gerhard, E Kominami, et al.

Acta Neurochirurgica|January 1, 1986

Hormone treatment of meningiomas: lack of response to medroxyprogesterone acetate (MPA). A pilot study of five casesJ Jääskeläinen, E Laasonen, J Kärkkäinen, et al.

American Journal of Medical Genetics|February 15, 1992

Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1pI Järvelä, P Santavuori, L Puhakka, et al.

Investigative Ophthalmology & Visual Science|September 1, 1994

Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndromeT Kivelä, A Tarkkanen, B Frangione, et al.

Surgical Neurology|March 1, 1985

Intracranial hemangiopericytoma: radiology, surgery, radiotherapy, and outcome in 21 patientsJ Jääskeläinen, A Servo, M Haltia, et al.

Acta Neuropathologica|January 1, 1988

A transient hypertensive opening of the blood-brain barrier can lead to brain damage. Extravasation of serum proteins and cellular changes in rats subjected to aortic compressionT E Sokrab, B B Johansson, H Kalimo, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|December 18, 2003

Mast cells and IgE-containing cells in gastric mucosa of Helicobacter pylori infected and non-infected patients with chronic urticariaM Liutu, K Kalimo, H Kalimo, et al.

Neuromuscular Disorders : NMD|October 1, 1996

Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutationT Tyni, A Majander, H Kalimo, et al.

Pageof 34