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John Paul Jones: An Overlooked Autopsy Finding that May Explain His Terminal Illness
John Paul Jones: An Overlooked Autopsy Finding that May Explain His Terminal Illness
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John Paul Jones: An Overlooked Autopsy Finding that May Explain His Terminal Illness

Hamrell, Burt B.

Journal of Forensic Sciences, 2016, Vol.61 (2), p.540-544

Blackwell Publishing Ltd

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2
From Bretonneau to therapeutic antibodies, from specificity to specific remedies, Saint-Cyr-Sur-Loire, France, November 19, 2012
From Bretonneau to therapeutic antibodies, from specificity to specific remedies, Saint-Cyr-Sur-Loire, France, November 19, 2012
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From Bretonneau to therapeutic antibodies, from specificity to specific remedies, Saint-Cyr-Sur-Loire, France, November 19, 2012

Marchand, Claire ; Nouat, Romaric ; Watier, Hervé

mAbs, 2013, Vol.5 (5), p.633-637

Taylor & Francis

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Immunohistochemical analysis of a ruptured basilar top aneurysm autopsied 22 years after embolization with Guglielmi detachable coils
Immunohistochemical analysis of a ruptured basilar top aneurysm autopsied 22 years after embolization with Guglielmi detachable coils
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Immunohistochemical analysis of a ruptured basilar top aneurysm autopsied 22 years after embolization with Guglielmi detachable coils

Yuki, Ichiro ; Spitzer, Daniel ; Guglielmi, Guido ; Duckwiler, Gary ; Fujimoto, Motoaki ; Takao, Hiroyuki ; Jahan, Reza ; Tateshima, Satoshi ; Murayama, Yuichi ; Vinuela, Fernando

BMJ Case Reports, 2014, Vol.2014

BMJ Publishing Group Ltd

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Hereditary neuropathy with liability to pressure palsies. Diagnosis in the first family (1947) confirmed
Hereditary neuropathy with liability to pressure palsies. Diagnosis in the first family (1947) confirmed
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Hereditary neuropathy with liability to pressure palsies. Diagnosis in the first family (1947) confirmed

Koehler, Peter J. ; Baas, Frank

Journal of the Peripheral Nervous System, 2012, Vol.17 (4), p.412-413

Malden, USA: Wiley Periodicals, Inc

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5
Coalition for the Advancement of Prosthetic Urology: History, Accomplishments, and Continuing Mission
Coalition for the Advancement of Prosthetic Urology: History, Accomplishments, and Continuing Mission
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Coalition for the Advancement of Prosthetic Urology: History, Accomplishments, and Continuing Mission

Daubert, Gail

The Journal of Sexual Medicine, 2006, Vol.3 (6), p.976-978

Malden, USA: Blackwell Publishing Inc

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6
Self-healing congenital verruciform hyperkeratosis
Self-healing congenital verruciform hyperkeratosis
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Self-healing congenital verruciform hyperkeratosis

Léauté-Labrèze, Christine ; Boralevi, Franck ; Cony, Mariane ; Maleville, Jean ; Lacombe, Didier ; Surlève-Bazeille, Jean-Etienne ; Taïeb, Alain

American Journal of Medical Genetics Part A, 2004, Vol.130A (3), p.303-306

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene
Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene
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Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene

Castori, Marco ; Ritelli, Marco ; Zoppi, Nicoletta ; Molisso, Luisa ; Chiarelli, Nicola ; Zaccagna, Fulvio ; Grammatico, Paola ; Colombi, Marina

American Journal of Medical Genetics Part A, 2012, Vol.158A (5), p.1164-1169

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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Jacobsen syndrome due to an unbalanced translocation between 11q23 and 22q11.2 identified at age 40 years
Jacobsen syndrome due to an unbalanced translocation between 11q23 and 22q11.2 identified at age 40 years
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Jacobsen syndrome due to an unbalanced translocation between 11q23 and 22q11.2 identified at age 40 years

Takahashi, Ikuko ; Takahashi, Tsutomu ; Sawada, Kenichi ; Shimojima, Keiko ; Yamamoto, Toshiyuki

American Journal of Medical Genetics Part A, 2012, Vol.158A (1), p.220-223

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
Novel DICER1 mutation as cause of multinodular goiter in children
Novel DICER1 mutation as cause of multinodular goiter in children
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Novel DICER1 mutation as cause of multinodular goiter in children

Darrat, Ilaaf ; Bedoyan, Jirair K. ; Chen, Ming ; Schuette, Jane L. ; Lesperance, Marci M.

Head & Neck, 2013, Vol.35 (12), p.E369-E371

Blackwell Publishing Ltd

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Obtaining a thorough sleep history and routinely screening for obstructive sleep apnea
Obtaining a thorough sleep history and routinely screening for obstructive sleep apnea
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Obtaining a thorough sleep history and routinely screening for obstructive sleep apnea

Lamm, Jamie ; Poeschel, Jane ; Smith, Sheila

Journal of the American Academy of Nurse Practitioners, 2008, Vol.20 (4), p.225-229

Malden, USA: Blackwell Publishing Inc

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