An Interactive Annotated World Bibliography of Printed and Digital Works in the History of Medicine and the Life Sciences from Circa 2000 BCE to Circa 2020 by Fielding H. Garrison (1870-1935), Leslie T. Morton (1907-2004), and Jeremy M. Norman (1945- ) Traditionally Known as “Garrison-Morton”

15478 entries, 13333 authors and 1903 subjects. Updated: December 6, 2021

MARIE, Pierre

9 entries
  • 3830

Sur la nature et sur quelques-uns des symptomes de la maladie de Basedow.

Arch. Neurol. (Paris), 6, 79-85, 1883.

The fourth cardinal sign in exophthalmic goitre – tremor – was first mentioned by Pierre Marie.



Subjects: ENDOCRINOLOGY › Thyroid
  • 4749

Sur une forme particuliére d’atrophie musculaire progressive souvent familiale débutant par les pieds et les jambes et atteignant plus tard les mains.

Rev. Méd., 6, 97-138, 1886.

First description of the peroneal form of muscular atrophy, the so-called Charcot–Marie–Tooth type.



Subjects: NEUROLOGY › Myopathies
  • 3884

Sur deux cas d’acromégalie. Hypertrophie singulière non congénitale des extrémités supérieures, inférieures et céphalique.

Rev. Méd., 6, 297-333, 1886.

In this, the first complete clinical description of the condition, Marie suggested the name “acromegaly”. The paper excited much interest and was translated into English and published by the New Sydenham Society, 1891.



Subjects: ENDOCRINOLOGY › Pituitary
  • 4354

De l’ostéo-arthropathie hypertrophiante pneumonique.

Rev. Méd., 10, 1-36, 1890.

Original description of hypertrophic osteoarthropathy, sometimes called “Bamberger–Marie disease”.



Subjects: ORTHOPEDICS › Diseases of or Injuries to Bones, Joints & Skeleton
  • 4708.1

Sur l’hérédo-ataxie cérébelleuse.

Sem. méd. (Paris), 13, 444-47, 1893.

Original description of hereditary cerebellar ataxia.



Subjects: GENETICS / HEREDITY › HEREDITARY / CONGENITAL DISEASES OR DISORDERS › Inherited Neurological Disorders › Hereditary Ataxias, NEUROLOGY › Degenerative Disorders
  • 4759

Existe-t-il une atrophie musculaire progressive Aran-Duchenne?

Rev. neurol. (Paris), 5, 686-90, 1897.

Marie disbelieved in the Aran–Duchenne type of muscular progressive atrophy.



Subjects: NEUROLOGY › Myopathies
  • 4368

Sur la Spondylose rhizomélique.

Rev. Méd., 18, 285-315, 1898.

Marie described as “spondylose rhizomélique” the ankylosing spondylitis or spondylitis deformans originally reported by Strümpell and called variously “Strümpell’s disease”, “Bechterev’s disease”, “Marie’s disease”.



Subjects: ORTHOPEDICS › Diseases of or Injuries to Bones, Joints & Skeleton, RHEUMATOLOGY
  • 4369

Sur la dysostose cléido-crânienne héréditaire.

Rev. neurol. (Paris), 6, 835-38, 1898.

In their important description of cleido-cranial dysostosis, Marie and Sainton gave to it its present name. It was first described by Morand (No. 4302.1) in 1760. English translation in Bick, Classics of orthopaedics, 230-32.



Subjects: GENETICS / HEREDITY › HEREDITARY / CONGENITAL DISEASES OR DISORDERS › Cranialfacial Disorders, ORTHOPEDICS › Diseases of or Injuries to Bones, Joints & Skeleton › Congenital Diseases , PLASTIC & RECONSTRUCTIVE SURGERY › Cranialfacial Surgery
  • 4630

Révision de la question de l’aphasie; la troisième circonvolution frontale gauche ne joue aucun rôle spécial dans la fonction du langage.

Sem. méd. (Paris), 26, 241-47, 1906.

Marie disputed Broca’s claim that the third left frontal convolution of the brain is the speech center. He classified aphasia into three groups: anarthria (defects of articulation), Broca’s (motor) aphasia, and Wernicke’s (sensory) aphasia.



Subjects: NEUROLOGY › Aphasia, Agraphia, Agnosia, Speech, Anatomy and Physiology of › Speech Disorders