«HEREDO-FAMILIAL» এর সঙ্গে সম্পর্কিত ইংরেজী বই
নিম্নলিখিত গ্রন্থপঞ্জী নির্বাচনে
heredo-familial শব্দটির ব্যবহার খুঁজুন। ইংরেজী সাহিত্যে
heredo-familial শব্দের ব্যবহারের প্রসঙ্গ সম্পর্কিত বই এবং তার থেকে সংক্ষিপ্তসার।
A large number of variant TTR proteins are thus known and form the amyloid
deposition in many heredo-familial amyloid diseases as well as in senile
amyloidoses. Amyloid Beta, Microglobulin (A(32M) This microglobulin is secreted
by the ...
2
Pediatric Neurology: A Color Handbook
Chronic, slowly progressive gait impairment with spasticity Disorders resulting in
this pattern of gait impairment are generally heredo-familial genetic disorders of
various types, although rare cases in children of neoplastic, paraneoplastic, and
...
James F Bale Jr, Joshua L Bonkowsky, Francis M Filloux,
2011
3
Neurological Practice: An Indian Perspective
An indigenous form of heredo-familial spinocerebellar degeneration with slow
eye movements. Neurol India 1973; 205: 561-80. 103. Starr A. A disorder of rapid
eye movements in Huntington's chorea. Brain 1967; 90: 545-64. 104. KulkarniSA
...
4
Cerebellar Degenerations: Clinical Neurobiology: Clinical ...
An indigenous form of heredo-familial spinocerebellar degeneration with slow
eye movements. Neurol. India Suppl. 1V:561-580. 148. Wadia N.H. (1977).
Heredo-familial spinocerebellar degeneration with slow eye movements —
Another ...
5
Eye Movement Disorders in Clinical Practice: Signs and Syndromes
A new form of heredo-familial spinocerebellar degeneration with slow eye
movements. Brain. 1971;94:359–374. Rub U, Brunt ER, Gierga K, Schultz C,
Paulson H, de Vos RAI, Braak H. The nucleus raphe interpositus in
spinocerebellar ataxia ...
6
Pathology of the Eye & Orbit
Table 5.5: Corneal dystrophies I-Epithelial I . r Heredo familial Corneal
Meesmann's Dystrophy — autosomal dominant —1-2 years — punctate les.ions
— increased basement membrane — increase in giycogen — diastase resistant
PAS ...
7
Genetic Disorders Among Arab Populations
Br J Dermatol 100(1):87–92 Muckle TJ, Wellsm (1962) Urticaria, deafness, and
amyloidosis: a new heredo-familial syndrome. Q J Med 31:235–248 Mulley J,
Saar K, Hewitt G, Ruschendorf F, Phillips H, Colley A, Sillence D, Reis A, Wilson
M ...
8
Primary Immunodeficiency Diseases: A Molecular and Cellular ...
AmJ Gastroenterol 2003;98: 2594–2604. Muckle TJ. The “Muckle-Wells”
syndrome. BrJ Dermatol 1979;100:87–92. Muckle TJ, Wells M. Urticaria,
deafness, and amyloidosis: a new heredo- familial syndrome. QJMed 1962;31:
235–248. Mulley ...
Hans D. Ochs,, C. I. Edvard Smith,, Jennifer M. Puck,,
2013
9
Pediatrics in Systemic Autoimmune Diseases
Tumour necrosis factor receptor associated periodic syndrome (TRAPS) with
central nervous system involvement. Ann. Rheum. Dis. 63 (10), 1356–1357.
Muckle, T.J., Wells, M. 1962. Urticaria, deafness and amyloidosis: a new heredo-
familial ...
Rolando Cimaz, Thomas J.A. Lehman,
2007
10
Emery and Rimoin's Principles and Practice of Medical Genetics
... M. Urticaria, Deafness and Amyloido— sis: A New Heredo—Familial Syndrome
. Med. 1962, 31, 235—248. Tindall, P.; Becker, S. K.; Rosse, W. F. Familial Cold
Urticaria: A Generalized Reaction Involving Leukocytosis. Arch. Intern. Med.
David L. Rimoin, Reed E. Pyeritz, Bruce Korf,
2013